Name: rs57445354
Published: September 21, 2022
License: Open Access

Welcome to the Reference SNP (rs) Report

All alleles are reported in the Forward orientation. Click on the Variant Details tab for details on Genomic Placement, Gene, and Amino Acid changes. HGVS names are in the HGVS tab.

Reference SNP (rs) Report

This page reports data for a single dbSNP Reference SNP variation (RefSNP or rs) from the new redesigned dbSNP build.
Top of the page reports a concise summary for the rs, with more specific details included in the corresponding tabs below.
All alleles are reported in the Forward orientation. Use the Genomic View to inspect the nucleotides flanking the variant, and its neighbors.
For more information see Help documentation.

rs57445354

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr6:33989507-33989530 (GRCh38.p14) Help
The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.
Alleles: del(TC)₄ / del(TC)₃ / delTCTC / de…
del(TC)₄ / del(TC)₃ / delTCTC / delTC / dupTC / dupTCTC / dup(TC)₃ / dup(TC)₄ / dup(TC)₅ / dup(TC)₆ / dup(TC)₇ / dup(TC)₈ / dup(TC)₉ / dup(TC)₁₀ / dup(TC)₁₁ / dup(TC)₁₂ / ins(TC)₁₃ / ins(TC)₁₄ / ins(TC)₁₅ / ins(TC)₁₆ / ins(TC)₁₇ / ins(TC)₁₈ / ins(TC)₁₉ / ins(TC)₂₀
Variation Type: Indel Insertion and Deletion
Frequency: dupTC=0.02463 (250/10149, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: None
Publications: 0 citations
Genomic View: See rs on genome

ALFA Allele Frequency
The ALFA project provide aggregate allele frequency from dbGaP. More information is available on the project page including descriptions, data access, and terms of use.

Release Version: 20230706150541

Population	Group	Sample Size	Ref Allele	Alt Allele
Total	Global	10149	TCTCTCTCTCTCTCTCTCTCTCTC=0.96019	TCTCTCTCTCTCTCTC=0.00000, TCTCTCTCTCTCTCTCTC=0.00000, TCTCTCTCTCTCTCTCTCTC=0.00000, TCTCTCTCTCTCTCTCTCTCTC=0.00000, TCTCTCTCTCTCTCTCTCTCTCTCTC=0.02463, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.01517, TCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.00000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.00000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.00000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.00000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.00000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.00000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.00000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.00000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.00000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.00000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.00000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.00000
European	Sub	8635	TCTCTCTCTCTCTCTCTCTCTCTC=0.9532	TCTCTCTCTCTCTCTC=0.0000, TCTCTCTCTCTCTCTCTC=0.0000, TCTCTCTCTCTCTCTCTCTC=0.0000, TCTCTCTCTCTCTCTCTCTCTC=0.0000, TCTCTCTCTCTCTCTCTCTCTCTCTC=0.0290, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.0178, TCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.0000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.0000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.0000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.0000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.0000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.0000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.0000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.0000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.0000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.0000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.0000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.0000
African	Sub	554	TCTCTCTCTCTCTCTCTCTCTCTC=1.000	TCTCTCTCTCTCTCTC=0.000, TCTCTCTCTCTCTCTCTC=0.000, TCTCTCTCTCTCTCTCTCTC=0.000, TCTCTCTCTCTCTCTCTCTCTC=0.000, TCTCTCTCTCTCTCTCTCTCTCTCTC=0.000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.000, TCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.000
African Others	Sub	22	TCTCTCTCTCTCTCTCTCTCTCTC=1.00	TCTCTCTCTCTCTCTC=0.00, TCTCTCTCTCTCTCTCTC=0.00, TCTCTCTCTCTCTCTCTCTC=0.00, TCTCTCTCTCTCTCTCTCTCTC=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTC=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.00
African American	Sub	532	TCTCTCTCTCTCTCTCTCTCTCTC=1.000	TCTCTCTCTCTCTCTC=0.000, TCTCTCTCTCTCTCTCTC=0.000, TCTCTCTCTCTCTCTCTCTC=0.000, TCTCTCTCTCTCTCTCTCTCTC=0.000, TCTCTCTCTCTCTCTCTCTCTCTCTC=0.000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.000, TCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.000
Asian	Sub	92	TCTCTCTCTCTCTCTCTCTCTCTC=1.00	TCTCTCTCTCTCTCTC=0.00, TCTCTCTCTCTCTCTCTC=0.00, TCTCTCTCTCTCTCTCTCTC=0.00, TCTCTCTCTCTCTCTCTCTCTC=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTC=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.00
East Asian	Sub	68	TCTCTCTCTCTCTCTCTCTCTCTC=1.00	TCTCTCTCTCTCTCTC=0.00, TCTCTCTCTCTCTCTCTC=0.00, TCTCTCTCTCTCTCTCTCTC=0.00, TCTCTCTCTCTCTCTCTCTCTC=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTC=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.00
Other Asian	Sub	24	TCTCTCTCTCTCTCTCTCTCTCTC=1.00	TCTCTCTCTCTCTCTC=0.00, TCTCTCTCTCTCTCTCTC=0.00, TCTCTCTCTCTCTCTCTCTC=0.00, TCTCTCTCTCTCTCTCTCTCTC=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTC=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.00
Latin American 1	Sub	76	TCTCTCTCTCTCTCTCTCTCTCTC=1.00	TCTCTCTCTCTCTCTC=0.00, TCTCTCTCTCTCTCTCTC=0.00, TCTCTCTCTCTCTCTCTCTC=0.00, TCTCTCTCTCTCTCTCTCTCTC=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTC=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.00
Latin American 2	Sub	456	TCTCTCTCTCTCTCTCTCTCTCTC=1.000	TCTCTCTCTCTCTCTC=0.000, TCTCTCTCTCTCTCTCTC=0.000, TCTCTCTCTCTCTCTCTCTC=0.000, TCTCTCTCTCTCTCTCTCTCTC=0.000, TCTCTCTCTCTCTCTCTCTCTCTCTC=0.000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.000, TCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.000
South Asian	Sub	74	TCTCTCTCTCTCTCTCTCTCTCTC=1.00	TCTCTCTCTCTCTCTC=0.00, TCTCTCTCTCTCTCTCTC=0.00, TCTCTCTCTCTCTCTCTCTC=0.00, TCTCTCTCTCTCTCTCTCTCTC=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTC=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.00, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.00
Other	Sub	262	TCTCTCTCTCTCTCTCTCTCTCTC=1.000	TCTCTCTCTCTCTCTC=0.000, TCTCTCTCTCTCTCTCTC=0.000, TCTCTCTCTCTCTCTCTCTC=0.000, TCTCTCTCTCTCTCTCTCTCTC=0.000, TCTCTCTCTCTCTCTCTCTCTCTCTC=0.000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.000, TCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.000, TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.000

Frequency tab displays a table of the reference and alternate allele frequencies reported by various studies and populations. Table lines, where Population="Global" refer to the entire study population, whereas lines, where Group="Sub", refer to a study-specific population subgroupings (i.e. AFR, CAU, etc.), if available. Frequency for the alternate allele (Alt Allele) is a ratio of samples observed-to-total, where the numerator (observed samples) is the number of chromosomes in the study with the minor allele present (found in "Sample size", where Group="Sub"), and the denominator (total samples) is the total number of all chromosomes in the study for the variant (found in "Sample size", where Group="Study-wide" and Population="Global").

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	10149	(TC)₁₂=0.96019	del(TC)₄=0.00000, del(TC)₃=0.00000, delTCTC=0.00000, delTC=0.00000, dupTC=0.02463, dupTCTC=0.00000, dup(TC)₃=0.00000, dup(TC)₄=0.00000, dup(TC)₅=0.00000, dup(TC)₆=0.01517, dup(TC)₇=0.00000, dup(TC)₈=0.00000, dup(TC)₉=0.00000, dup(TC)₁₀=0.00000, dup(TC)₁₁=0.00000, dup(TC)₁₂=0.00000, ins(TC)₁₃=0.00000, ins(TC)₁₄=0.00000
Allele Frequency Aggregator	European	Sub	8635	(TC)₁₂=0.9532	del(TC)₄=0.0000, del(TC)₃=0.0000, delTCTC=0.0000, delTC=0.0000, dupTC=0.0290, dupTCTC=0.0000, dup(TC)₃=0.0000, dup(TC)₄=0.0000, dup(TC)₅=0.0000, dup(TC)₆=0.0178, dup(TC)₇=0.0000, dup(TC)₈=0.0000, dup(TC)₉=0.0000, dup(TC)₁₀=0.0000, dup(TC)₁₁=0.0000, dup(TC)₁₂=0.0000, ins(TC)₁₃=0.0000, ins(TC)₁₄=0.0000
Allele Frequency Aggregator	African	Sub	554	(TC)₁₂=1.000	del(TC)₄=0.000, del(TC)₃=0.000, delTCTC=0.000, delTC=0.000, dupTC=0.000, dupTCTC=0.000, dup(TC)₃=0.000, dup(TC)₄=0.000, dup(TC)₅=0.000, dup(TC)₆=0.000, dup(TC)₇=0.000, dup(TC)₈=0.000, dup(TC)₉=0.000, dup(TC)₁₀=0.000, dup(TC)₁₁=0.000, dup(TC)₁₂=0.000, ins(TC)₁₃=0.000, ins(TC)₁₄=0.000
Allele Frequency Aggregator	Latin American 2	Sub	456	(TC)₁₂=1.000	del(TC)₄=0.000, del(TC)₃=0.000, delTCTC=0.000, delTC=0.000, dupTC=0.000, dupTCTC=0.000, dup(TC)₃=0.000, dup(TC)₄=0.000, dup(TC)₅=0.000, dup(TC)₆=0.000, dup(TC)₇=0.000, dup(TC)₈=0.000, dup(TC)₉=0.000, dup(TC)₁₀=0.000, dup(TC)₁₁=0.000, dup(TC)₁₂=0.000, ins(TC)₁₃=0.000, ins(TC)₁₄=0.000
Allele Frequency Aggregator	Other	Sub	262	(TC)₁₂=1.000	del(TC)₄=0.000, del(TC)₃=0.000, delTCTC=0.000, delTC=0.000, dupTC=0.000, dupTCTC=0.000, dup(TC)₃=0.000, dup(TC)₄=0.000, dup(TC)₅=0.000, dup(TC)₆=0.000, dup(TC)₇=0.000, dup(TC)₈=0.000, dup(TC)₉=0.000, dup(TC)₁₀=0.000, dup(TC)₁₁=0.000, dup(TC)₁₂=0.000, ins(TC)₁₃=0.000, ins(TC)₁₄=0.000
Allele Frequency Aggregator	Asian	Sub	92	(TC)₁₂=1.00	del(TC)₄=0.00, del(TC)₃=0.00, delTCTC=0.00, delTC=0.00, dupTC=0.00, dupTCTC=0.00, dup(TC)₃=0.00, dup(TC)₄=0.00, dup(TC)₅=0.00, dup(TC)₆=0.00, dup(TC)₇=0.00, dup(TC)₈=0.00, dup(TC)₉=0.00, dup(TC)₁₀=0.00, dup(TC)₁₁=0.00, dup(TC)₁₂=0.00, ins(TC)₁₃=0.00, ins(TC)₁₄=0.00
Allele Frequency Aggregator	Latin American 1	Sub	76	(TC)₁₂=1.00	del(TC)₄=0.00, del(TC)₃=0.00, delTCTC=0.00, delTC=0.00, dupTC=0.00, dupTCTC=0.00, dup(TC)₃=0.00, dup(TC)₄=0.00, dup(TC)₅=0.00, dup(TC)₆=0.00, dup(TC)₇=0.00, dup(TC)₈=0.00, dup(TC)₉=0.00, dup(TC)₁₀=0.00, dup(TC)₁₁=0.00, dup(TC)₁₂=0.00, ins(TC)₁₃=0.00, ins(TC)₁₄=0.00
Allele Frequency Aggregator	South Asian	Sub	74	(TC)₁₂=1.00	del(TC)₄=0.00, del(TC)₃=0.00, delTCTC=0.00, delTC=0.00, dupTC=0.00, dupTCTC=0.00, dup(TC)₃=0.00, dup(TC)₄=0.00, dup(TC)₅=0.00, dup(TC)₆=0.00, dup(TC)₇=0.00, dup(TC)₈=0.00, dup(TC)₉=0.00, dup(TC)₁₀=0.00, dup(TC)₁₁=0.00, dup(TC)₁₂=0.00, ins(TC)₁₃=0.00, ins(TC)₁₄=0.00

Variant Details tab shows known variant placements on genomic sequences: chromosomes (NC_), RefSeqGene, pseudogenes or genomic regions (NG_), and in a separate table: on transcripts (NM_) and protein sequences (NP_). The corresponding transcript and protein locations are listed in adjacent lines, along with molecular consequences from Sequence Ontology. When no protein placement is available, only the transcript is listed. Column "Codon[Amino acid]" shows the actual base change in the format of "Reference > Alternate" allele, including the nucleotide codon change in transcripts, and the amino acid change in proteins, respectively, allowing for known ribosomal slippage sites. To view nucleotides adjacent to the variant use the Genomic View at the bottom of the page - zoom into the sequence until the nucleotides around the variant become visible.

Genomic Placements

Sequence name	Change
GRCh38.p14 chr 6	NC_000006.12:g.33989507TC[8]
GRCh38.p14 chr 6	NC_000006.12:g.33989507TC[9]
GRCh38.p14 chr 6	NC_000006.12:g.33989507TC[10]
GRCh38.p14 chr 6	NC_000006.12:g.33989507TC[11]
GRCh38.p14 chr 6	NC_000006.12:g.33989507TC[13]
GRCh38.p14 chr 6	NC_000006.12:g.33989507TC[14]
GRCh38.p14 chr 6	NC_000006.12:g.33989507TC[15]
GRCh38.p14 chr 6	NC_000006.12:g.33989507TC[16]
GRCh38.p14 chr 6	NC_000006.12:g.33989507TC[17]
GRCh38.p14 chr 6	NC_000006.12:g.33989507TC[18]
GRCh38.p14 chr 6	NC_000006.12:g.33989507TC[19]
GRCh38.p14 chr 6	NC_000006.12:g.33989507TC[20]
GRCh38.p14 chr 6	NC_000006.12:g.33989507TC[21]
GRCh38.p14 chr 6	NC_000006.12:g.33989507TC[22]
GRCh38.p14 chr 6	NC_000006.12:g.33989507TC[23]
GRCh38.p14 chr 6	NC_000006.12:g.33989507TC[24]
GRCh38.p14 chr 6	NC_000006.12:g.33989507TC[25]
GRCh38.p14 chr 6	NC_000006.12:g.33989507TC[26]
GRCh38.p14 chr 6	NC_000006.12:g.33989507TC[27]
GRCh38.p14 chr 6	NC_000006.12:g.33989507TC[28]
GRCh38.p14 chr 6	NC_000006.12:g.33989507TC[29]
GRCh38.p14 chr 6	NC_000006.12:g.33989507TC[30]
GRCh38.p14 chr 6	NC_000006.12:g.33989507TC[31]
GRCh38.p14 chr 6	NC_000006.12:g.33989507TC[32]
GRCh37.p13 chr 6	NC_000006.11:g.33957284TC[8]
GRCh37.p13 chr 6	NC_000006.11:g.33957284TC[9]
GRCh37.p13 chr 6	NC_000006.11:g.33957284TC[10]
GRCh37.p13 chr 6	NC_000006.11:g.33957284TC[11]
GRCh37.p13 chr 6	NC_000006.11:g.33957284TC[13]
GRCh37.p13 chr 6	NC_000006.11:g.33957284TC[14]
GRCh37.p13 chr 6	NC_000006.11:g.33957284TC[15]
GRCh37.p13 chr 6	NC_000006.11:g.33957284TC[16]
GRCh37.p13 chr 6	NC_000006.11:g.33957284TC[17]
GRCh37.p13 chr 6	NC_000006.11:g.33957284TC[18]
GRCh37.p13 chr 6	NC_000006.11:g.33957284TC[19]
GRCh37.p13 chr 6	NC_000006.11:g.33957284TC[20]
GRCh37.p13 chr 6	NC_000006.11:g.33957284TC[21]
GRCh37.p13 chr 6	NC_000006.11:g.33957284TC[22]
GRCh37.p13 chr 6	NC_000006.11:g.33957284TC[23]
GRCh37.p13 chr 6	NC_000006.11:g.33957284TC[24]
GRCh37.p13 chr 6	NC_000006.11:g.33957284TC[25]
GRCh37.p13 chr 6	NC_000006.11:g.33957284TC[26]
GRCh37.p13 chr 6	NC_000006.11:g.33957284TC[27]
GRCh37.p13 chr 6	NC_000006.11:g.33957284TC[28]
GRCh37.p13 chr 6	NC_000006.11:g.33957284TC[29]
GRCh37.p13 chr 6	NC_000006.11:g.33957284TC[30]
GRCh37.p13 chr 6	NC_000006.11:g.33957284TC[31]
GRCh37.p13 chr 6	NC_000006.11:g.33957284TC[32]

Clinical Significance tab shows a list of clinical significance entries from ClinVar associated with the variation, per allele. Click on the RCV accession (i.e. RCV000001615.2) or Allele ID (i.e. 12274) to access full ClinVar report.

Not Reported in ClinVar

Aliases tab displays HGVS names representing the variant placements and allele changes on genomic, transcript and protein sequences, per allele. HGVS name is an expression for reporting sequence accession and version, sequence type, position, and allele change. The column "Note" can have two values: "diff" means that there is a difference between the reference allele (variation interval) at the placement reported in HGVS name and the reference alleles reported in other HGVS names, and "rev" means that the sequence of this variation interval at the placement reported in HGVS name is in reverse orientation to the sequence(s) of this variation in other HGVS names not labeled as "rev".

Placement	(TC)₁₂=	del(TC)₄	del(TC)₃	delTCTC	delTC	dupTC	dupTCTC	dup(TC)₃	dup(TC)₄	dup(TC)₅	dup(TC)₆	dup(TC)₇	dup(TC)₈	dup(TC)₉	dup(TC)₁₀	dup(TC)₁₁	dup(TC)₁₂	ins(TC)₁₃	ins(TC)₁₄	ins(TC)₁₅	ins(TC)₁₆	ins(TC)₁₇	ins(TC)₁₈	ins(TC)₁₉	ins(TC)₂₀
GRCh38.p14 chr 6	NC_000006.12:g.33989507_33989530=	NC_000006.12:g.33989507TC[8]	NC_000006.12:g.33989507TC[9]	NC_000006.12:g.33989507TC[10]	NC_000006.12:g.33989507TC[11]	NC_000006.12:g.33989507TC[13]	NC_000006.12:g.33989507TC[14]	NC_000006.12:g.33989507TC[15]	NC_000006.12:g.33989507TC[16]	NC_000006.12:g.33989507TC[17]	NC_000006.12:g.33989507TC[18]	NC_000006.12:g.33989507TC[19]	NC_000006.12:g.33989507TC[20]	NC_000006.12:g.33989507TC[21]	NC_000006.12:g.33989507TC[22]	NC_000006.12:g.33989507TC[23]	NC_000006.12:g.33989507TC[24]	NC_000006.12:g.33989507TC[25]	NC_000006.12:g.33989507TC[26]	NC_000006.12:g.33989507TC[27]	NC_000006.12:g.33989507TC[28]	NC_000006.12:g.33989507TC[29]	NC_000006.12:g.33989507TC[30]	NC_000006.12:g.33989507TC[31]	NC_000006.12:g.33989507TC[32]
GRCh37.p13 chr 6	NC_000006.11:g.33957284_33957307=	NC_000006.11:g.33957284TC[8]	NC_000006.11:g.33957284TC[9]	NC_000006.11:g.33957284TC[10]	NC_000006.11:g.33957284TC[11]	NC_000006.11:g.33957284TC[13]	NC_000006.11:g.33957284TC[14]	NC_000006.11:g.33957284TC[15]	NC_000006.11:g.33957284TC[16]	NC_000006.11:g.33957284TC[17]	NC_000006.11:g.33957284TC[18]	NC_000006.11:g.33957284TC[19]	NC_000006.11:g.33957284TC[20]	NC_000006.11:g.33957284TC[21]	NC_000006.11:g.33957284TC[22]	NC_000006.11:g.33957284TC[23]	NC_000006.11:g.33957284TC[24]	NC_000006.11:g.33957284TC[25]	NC_000006.11:g.33957284TC[26]	NC_000006.11:g.33957284TC[27]	NC_000006.11:g.33957284TC[28]	NC_000006.11:g.33957284TC[29]	NC_000006.11:g.33957284TC[30]	NC_000006.11:g.33957284TC[31]	NC_000006.11:g.33957284TC[32]

Submissions tab displays variations originally submitted to dbSNP, now supporting this RefSNP cluster (rs). We display Submitter handle, Submission identifier, Date and Build number, when the submission appeared for the first time. Direct submissions to dbSNP have Submission ID in the form of an ss-prefixed number (ss#). Other supporting variations are listed in the table without ss#.

36 SubSNP, 26 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss79994164	Dec 14, 2007 (129)
2	HGSV	ss82328399	Dec 14, 2007 (129)
3	1000GENOMES	ss327082015	May 09, 2011 (134)
4	SSMP	ss663690812	Apr 01, 2015 (144)
5	SWEGEN	ss2998863844	Nov 08, 2017 (151)
6	SWEGEN	ss2998863845	Nov 08, 2017 (151)
7	MCHAISSO	ss3064200371	Nov 08, 2017 (151)
8	MCHAISSO	ss3066074956	Nov 08, 2017 (151)
9	URBANLAB	ss3648325632	Oct 12, 2018 (152)
10	KHV_HUMAN_GENOMES	ss3808019834	Jul 13, 2019 (153)
11	EVA	ss3829860393	Apr 26, 2020 (154)
12	GNOMAD	ss4139647053	Apr 26, 2021 (155)
13	GNOMAD	ss4139647054	Apr 26, 2021 (155)
14	GNOMAD	ss4139647055	Apr 26, 2021 (155)
15	GNOMAD	ss4139647056	Apr 26, 2021 (155)
16	GNOMAD	ss4139647057	Apr 26, 2021 (155)
17	GNOMAD	ss4139647058	Apr 26, 2021 (155)
18	GNOMAD	ss4139647059	Apr 26, 2021 (155)
19	GNOMAD	ss4139647061	Apr 26, 2021 (155)
20	GNOMAD	ss4139647071	Apr 26, 2021 (155)
21	GNOMAD	ss4139647074	Apr 26, 2021 (155)
22	GNOMAD	ss4139647075	Apr 26, 2021 (155)
23	GNOMAD	ss4139647076	Apr 26, 2021 (155)
24	GNOMAD	ss4139647077	Apr 26, 2021 (155)
25	GNOMAD	ss4139647078	Apr 26, 2021 (155)
26	GNOMAD	ss4139647079	Apr 26, 2021 (155)
27	GNOMAD	ss4139647080	Apr 26, 2021 (155)
28	GNOMAD	ss4139647081	Apr 26, 2021 (155)
29	GNOMAD	ss4139647082	Apr 26, 2021 (155)
30	GNOMAD	ss4139647083	Apr 26, 2021 (155)
31	GNOMAD	ss4139647084	Apr 26, 2021 (155)
32	GNOMAD	ss4139647102	Apr 26, 2021 (155)
33	GNOMAD	ss4139647103	Apr 26, 2021 (155)
34	GNOMAD	ss4139647104	Apr 26, 2021 (155)
35	TOMMO_GENOMICS	ss5714840510	Oct 13, 2022 (156)
36	TOMMO_GENOMICS	ss5714840514	Oct 13, 2022 (156)
37	gnomAD - Genomes Submission ignored due to conflicting rows: Row 221684514 (NC_000006.12:33989506::TC 1493/130216) Row 221684515 (NC_000006.12:33989506::TCTC 589/130226) Row 221684516 (NC_000006.12:33989506::TCTCTC 5476/130206)...	-	Apr 26, 2021 (155)
38	gnomAD - Genomes Submission ignored due to conflicting rows: Row 221684514 (NC_000006.12:33989506::TC 1493/130216) Row 221684515 (NC_000006.12:33989506::TCTC 589/130226) Row 221684516 (NC_000006.12:33989506::TCTCTC 5476/130206)...	-	Apr 26, 2021 (155)
39	gnomAD - Genomes Submission ignored due to conflicting rows: Row 221684514 (NC_000006.12:33989506::TC 1493/130216) Row 221684515 (NC_000006.12:33989506::TCTC 589/130226) Row 221684516 (NC_000006.12:33989506::TCTCTC 5476/130206)...	-	Apr 26, 2021 (155)
40	gnomAD - Genomes Submission ignored due to conflicting rows: Row 221684514 (NC_000006.12:33989506::TC 1493/130216) Row 221684515 (NC_000006.12:33989506::TCTC 589/130226) Row 221684516 (NC_000006.12:33989506::TCTCTC 5476/130206)...	-	Apr 26, 2021 (155)
41	gnomAD - Genomes Submission ignored due to conflicting rows: Row 221684514 (NC_000006.12:33989506::TC 1493/130216) Row 221684515 (NC_000006.12:33989506::TCTC 589/130226) Row 221684516 (NC_000006.12:33989506::TCTCTC 5476/130206)...	-	Apr 26, 2021 (155)
42	gnomAD - Genomes Submission ignored due to conflicting rows: Row 221684514 (NC_000006.12:33989506::TC 1493/130216) Row 221684515 (NC_000006.12:33989506::TCTC 589/130226) Row 221684516 (NC_000006.12:33989506::TCTCTC 5476/130206)...	-	Apr 26, 2021 (155)
43	gnomAD - Genomes Submission ignored due to conflicting rows: Row 221684514 (NC_000006.12:33989506::TC 1493/130216) Row 221684515 (NC_000006.12:33989506::TCTC 589/130226) Row 221684516 (NC_000006.12:33989506::TCTCTC 5476/130206)...	-	Apr 26, 2021 (155)
44	gnomAD - Genomes Submission ignored due to conflicting rows: Row 221684514 (NC_000006.12:33989506::TC 1493/130216) Row 221684515 (NC_000006.12:33989506::TCTC 589/130226) Row 221684516 (NC_000006.12:33989506::TCTCTC 5476/130206)...	-	Apr 26, 2021 (155)
45	gnomAD - Genomes Submission ignored due to conflicting rows: Row 221684514 (NC_000006.12:33989506::TC 1493/130216) Row 221684515 (NC_000006.12:33989506::TCTC 589/130226) Row 221684516 (NC_000006.12:33989506::TCTCTC 5476/130206)...	-	Apr 26, 2021 (155)
46	gnomAD - Genomes Submission ignored due to conflicting rows: Row 221684514 (NC_000006.12:33989506::TC 1493/130216) Row 221684515 (NC_000006.12:33989506::TCTC 589/130226) Row 221684516 (NC_000006.12:33989506::TCTCTC 5476/130206)...	-	Apr 26, 2021 (155)
47	gnomAD - Genomes Submission ignored due to conflicting rows: Row 221684514 (NC_000006.12:33989506::TC 1493/130216) Row 221684515 (NC_000006.12:33989506::TCTC 589/130226) Row 221684516 (NC_000006.12:33989506::TCTCTC 5476/130206)...	-	Apr 26, 2021 (155)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 221684514 (NC_000006.12:33989506::TC 1493/130216) Row 221684515 (NC_000006.12:33989506::TCTC 589/130226) Row 221684516 (NC_000006.12:33989506::TCTCTC 5476/130206)...	-	Apr 26, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 221684514 (NC_000006.12:33989506::TC 1493/130216) Row 221684515 (NC_000006.12:33989506::TCTC 589/130226) Row 221684516 (NC_000006.12:33989506::TCTCTC 5476/130206)...	-	Apr 26, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 221684514 (NC_000006.12:33989506::TC 1493/130216) Row 221684515 (NC_000006.12:33989506::TCTC 589/130226) Row 221684516 (NC_000006.12:33989506::TCTCTC 5476/130206)...	-	Apr 26, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 221684514 (NC_000006.12:33989506::TC 1493/130216) Row 221684515 (NC_000006.12:33989506::TCTC 589/130226) Row 221684516 (NC_000006.12:33989506::TCTCTC 5476/130206)...	-	Apr 26, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 221684514 (NC_000006.12:33989506::TC 1493/130216) Row 221684515 (NC_000006.12:33989506::TCTC 589/130226) Row 221684516 (NC_000006.12:33989506::TCTCTC 5476/130206)...	-	Apr 26, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 221684514 (NC_000006.12:33989506::TC 1493/130216) Row 221684515 (NC_000006.12:33989506::TCTC 589/130226) Row 221684516 (NC_000006.12:33989506::TCTCTC 5476/130206)...	-	Apr 26, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 221684514 (NC_000006.12:33989506::TC 1493/130216) Row 221684515 (NC_000006.12:33989506::TCTC 589/130226) Row 221684516 (NC_000006.12:33989506::TCTCTC 5476/130206)...	-	Apr 26, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 221684514 (NC_000006.12:33989506::TC 1493/130216) Row 221684515 (NC_000006.12:33989506::TCTC 589/130226) Row 221684516 (NC_000006.12:33989506::TCTCTC 5476/130206)...	-	Apr 26, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 221684514 (NC_000006.12:33989506::TC 1493/130216) Row 221684515 (NC_000006.12:33989506::TCTC 589/130226) Row 221684516 (NC_000006.12:33989506::TCTCTC 5476/130206)...	-	Apr 26, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 221684514 (NC_000006.12:33989506::TC 1493/130216) Row 221684515 (NC_000006.12:33989506::TCTC 589/130226) Row 221684516 (NC_000006.12:33989506::TCTCTC 5476/130206)...	-	Apr 26, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 221684514 (NC_000006.12:33989506::TC 1493/130216) Row 221684515 (NC_000006.12:33989506::TCTC 589/130226) Row 221684516 (NC_000006.12:33989506::TCTCTC 5476/130206)...	-	Apr 26, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 221684514 (NC_000006.12:33989506::TC 1493/130216) Row 221684515 (NC_000006.12:33989506::TCTC 589/130226) Row 221684516 (NC_000006.12:33989506::TCTCTC 5476/130206)...	-	Apr 26, 2021 (155)
60	14KJPN Submission ignored due to conflicting rows: Row 48677614 (NC_000006.12:33989506::TC 1619/28248) Row 48677618 (NC_000006.12:33989506::TCTCTCTCTCTCTCTCTCTCTCTC 953/28248)	-	Oct 13, 2022 (156)
61	14KJPN Submission ignored due to conflicting rows: Row 48677614 (NC_000006.12:33989506::TC 1619/28248) Row 48677618 (NC_000006.12:33989506::TCTCTCTCTCTCTCTCTCTCTCTC 953/28248)	-	Oct 13, 2022 (156)
62	ALFA	NC_000006.12 - 33989507	Apr 26, 2021 (155)

History tab displays RefSNPs (Associated ID) from previous builds (Build) that now support the current RefSNP, and the dates, when the history was updated for each Associated ID (History Updated).

Associated ID	History Updated (Build)
rs145330666	Oct 19, 2011 (136)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4139647104	NC_000006.12:33989506:TCTCTCTC:	NC_000006.12:33989506:TCTCTCTCTCTC… NC_000006.12:33989506:TCTCTCTCTCTCTCTCTCTCTCTC:TCTCTCTCTCTCTCTC	(self)
1360588916	NC_000006.12:33989506:TCTCTCTCTCTC… NC_000006.12:33989506:TCTCTCTCTCTCTCTCTCTCTCTC:TCTCTCTCTCTCTCTC	NC_000006.12:33989506:TCTCTCTCTCTC… NC_000006.12:33989506:TCTCTCTCTCTCTCTCTCTCTCTC:TCTCTCTCTCTCTCTC	(self)
1360588916	NC_000006.12:33989506:TCTCTCTCTCTC… NC_000006.12:33989506:TCTCTCTCTCTCTCTCTCTCTCTC:TCTCTCTCTCTCTCTCTC	NC_000006.12:33989506:TCTCTCTCTCTC… NC_000006.12:33989506:TCTCTCTCTCTCTCTCTCTCTCTC:TCTCTCTCTCTCTCTCTC	(self)
ss4139647103	NC_000006.12:33989506:TCTC:	NC_000006.12:33989506:TCTCTCTCTCTC… NC_000006.12:33989506:TCTCTCTCTCTCTCTCTCTCTCTC:TCTCTCTCTCTCTCTCTCTC	(self)
1360588916	NC_000006.12:33989506:TCTCTCTCTCTC… NC_000006.12:33989506:TCTCTCTCTCTCTCTCTCTCTCTC:TCTCTCTCTCTCTCTCTCTC	NC_000006.12:33989506:TCTCTCTCTCTC… NC_000006.12:33989506:TCTCTCTCTCTCTCTCTCTCTCTC:TCTCTCTCTCTCTCTCTCTC	(self)
ss663690812	NC_000006.11:33957283:TC:	NC_000006.12:33989506:TCTCTCTCTCTC… NC_000006.12:33989506:TCTCTCTCTCTCTCTCTCTCTCTC:TCTCTCTCTCTCTCTCTCTCTC	(self)
ss3808019834, ss4139647102	NC_000006.12:33989506:TC:	NC_000006.12:33989506:TCTCTCTCTCTC… NC_000006.12:33989506:TCTCTCTCTCTCTCTCTCTCTCTC:TCTCTCTCTCTCTCTCTCTCTC	(self)
1360588916	NC_000006.12:33989506:TCTCTCTCTCTC… NC_000006.12:33989506:TCTCTCTCTCTCTCTCTCTCTCTC:TCTCTCTCTCTCTCTCTCTCTC	NC_000006.12:33989506:TCTCTCTCTCTC… NC_000006.12:33989506:TCTCTCTCTCTCTCTCTCTCTCTC:TCTCTCTCTCTCTCTCTCTCTC	(self)
ss2998863845	NC_000006.11:33957283::TC	NC_000006.12:33989506:TCTCTCTCTCTC… NC_000006.12:33989506:TCTCTCTCTCTCTCTCTCTCTCTC:TCTCTCTCTCTCTCTCTCTCTCTCTC	(self)
ss3064200371, ss4139647053, ss5714840510	NC_000006.12:33989506::TC	NC_000006.12:33989506:TCTCTCTCTCTC… NC_000006.12:33989506:TCTCTCTCTCTCTCTCTCTCTCTC:TCTCTCTCTCTCTCTCTCTCTCTCTC	(self)
1360588916	NC_000006.12:33989506:TCTCTCTCTCTC… NC_000006.12:33989506:TCTCTCTCTCTCTCTCTCTCTCTC:TCTCTCTCTCTCTCTCTCTCTCTCTC	NC_000006.12:33989506:TCTCTCTCTCTC… NC_000006.12:33989506:TCTCTCTCTCTCTCTCTCTCTCTC:TCTCTCTCTCTCTCTCTCTCTCTCTC	(self)
ss4139647054	NC_000006.12:33989506::TCTC	NC_000006.12:33989506:TCTCTCTCTCTC… NC_000006.12:33989506:TCTCTCTCTCTCTCTCTCTCTCTC:TCTCTCTCTCTCTCTCTCTCTCTCTCTC	(self)
1360588916	NC_000006.12:33989506:TCTCTCTCTCTC… NC_000006.12:33989506:TCTCTCTCTCTCTCTCTCTCTCTC:TCTCTCTCTCTCTCTCTCTCTCTCTCTC	NC_000006.12:33989506:TCTCTCTCTCTC… NC_000006.12:33989506:TCTCTCTCTCTCTCTCTCTCTCTC:TCTCTCTCTCTCTCTCTCTCTCTCTCTC	(self)
ss327082015	NC_000006.10:34065261::TCTCTC	NC_000006.12:33989506:TCTCTCTCTCTC… NC_000006.12:33989506:TCTCTCTCTCTCTCTCTCTCTCTC:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTC	(self)
ss3066074956, ss4139647055	NC_000006.12:33989506::TCTCTC	NC_000006.12:33989506:TCTCTCTCTCTC… NC_000006.12:33989506:TCTCTCTCTCTCTCTCTCTCTCTC:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTC	(self)
1360588916	NC_000006.12:33989506:TCTCTCTCTCTC… NC_000006.12:33989506:TCTCTCTCTCTCTCTCTCTCTCTC:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTC	NC_000006.12:33989506:TCTCTCTCTCTC… NC_000006.12:33989506:TCTCTCTCTCTCTCTCTCTCTCTC:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTC	(self)
ss82328399	NT_007592.15:33897307::TCTCTC	NC_000006.12:33989506:TCTCTCTCTCTC… NC_000006.12:33989506:TCTCTCTCTCTCTCTCTCTCTCTC:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTC	(self)
ss4139647056	NC_000006.12:33989506::TCTCTCTC	NC_000006.12:33989506:TCTCTCTCTCTC… NC_000006.12:33989506:TCTCTCTCTCTCTCTCTCTCTCTC:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC	(self)
1360588916	NC_000006.12:33989506:TCTCTCTCTCTC… NC_000006.12:33989506:TCTCTCTCTCTCTCTCTCTCTCTC:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC	NC_000006.12:33989506:TCTCTCTCTCTC… NC_000006.12:33989506:TCTCTCTCTCTCTCTCTCTCTCTC:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC	(self)
ss4139647057	NC_000006.12:33989506::TCTCTCTCTC	NC_000006.12:33989506:TCTCTCTCTCTC… NC_000006.12:33989506:TCTCTCTCTCTCTCTCTCTCTCTC:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC	(self)
1360588916	NC_000006.12:33989506:TCTCTCTCTCTC… NC_000006.12:33989506:TCTCTCTCTCTCTCTCTCTCTCTC:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC	NC_000006.12:33989506:TCTCTCTCTCTC… NC_000006.12:33989506:TCTCTCTCTCTCTCTCTCTCTCTC:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC	(self)
ss3648325632	NC_000006.12:33989528::TCTCTCTCTC	NC_000006.12:33989506:TCTCTCTCTCTC… NC_000006.12:33989506:TCTCTCTCTCTCTCTCTCTCTCTC:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC	(self)
ss2998863844, ss3829860393	NC_000006.11:33957283::TCTCTCTCTCTC	NC_000006.12:33989506:TCTCTCTCTCTC… NC_000006.12:33989506:TCTCTCTCTCTCTCTCTCTCTCTC:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC	(self)
ss4139647058	NC_000006.12:33989506::TCTCTCTCTCTC	NC_000006.12:33989506:TCTCTCTCTCTC… NC_000006.12:33989506:TCTCTCTCTCTCTCTCTCTCTCTC:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC	(self)
1360588916	NC_000006.12:33989506:TCTCTCTCTCTC… NC_000006.12:33989506:TCTCTCTCTCTCTCTCTCTCTCTC:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC	NC_000006.12:33989506:TCTCTCTCTCTC… NC_000006.12:33989506:TCTCTCTCTCTCTCTCTCTCTCTC:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC	(self)
ss79994164	NT_007592.15:33897307::TCTCTCTCTCTC	NC_000006.12:33989506:TCTCTCTCTCTC… NC_000006.12:33989506:TCTCTCTCTCTCTCTCTCTCTCTC:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC	(self)
ss4139647059	NC_000006.12:33989506::TCTCTCTCTCT… NC_000006.12:33989506::TCTCTCTCTCTCTC	NC_000006.12:33989506:TCTCTCTCTCTC… NC_000006.12:33989506:TCTCTCTCTCTCTCTCTCTCTCTC:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC	(self)
1360588916	NC_000006.12:33989506:TCTCTCTCTCTC… NC_000006.12:33989506:TCTCTCTCTCTCTCTCTCTCTCTC:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC	NC_000006.12:33989506:TCTCTCTCTCTC… NC_000006.12:33989506:TCTCTCTCTCTCTCTCTCTCTCTC:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC	(self)
ss4139647061	NC_000006.12:33989506::TCTCTCTCTCT… NC_000006.12:33989506::TCTCTCTCTCTCTCTC	NC_000006.12:33989506:TCTCTCTCTCTC… NC_000006.12:33989506:TCTCTCTCTCTCTCTCTCTCTCTC:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC	(self)
1360588916	NC_000006.12:33989506:TCTCTCTCTCTC… NC_000006.12:33989506:TCTCTCTCTCTCTCTCTCTCTCTC:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC	NC_000006.12:33989506:TCTCTCTCTCTC… NC_000006.12:33989506:TCTCTCTCTCTCTCTCTCTCTCTC:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC	(self)
ss4139647071	NC_000006.12:33989506::TCTCTCTCTCT… NC_000006.12:33989506::TCTCTCTCTCTCTCTCTC	NC_000006.12:33989506:TCTCTCTCTCTC… NC_000006.12:33989506:TCTCTCTCTCTCTCTCTCTCTCTC:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC	(self)
1360588916	NC_000006.12:33989506:TCTCTCTCTCTC… NC_000006.12:33989506:TCTCTCTCTCTCTCTCTCTCTCTC:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC	NC_000006.12:33989506:TCTCTCTCTCTC… NC_000006.12:33989506:TCTCTCTCTCTCTCTCTCTCTCTC:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC	(self)
ss4139647074	NC_000006.12:33989506::TCTCTCTCTCT… NC_000006.12:33989506::TCTCTCTCTCTCTCTCTCTC	NC_000006.12:33989506:TCTCTCTCTCTC… NC_000006.12:33989506:TCTCTCTCTCTCTCTCTCTCTCTC:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC	(self)
1360588916	NC_000006.12:33989506:TCTCTCTCTCTC… NC_000006.12:33989506:TCTCTCTCTCTCTCTCTCTCTCTC:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC	NC_000006.12:33989506:TCTCTCTCTCTC… NC_000006.12:33989506:TCTCTCTCTCTCTCTCTCTCTCTC:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC	(self)
ss4139647075	NC_000006.12:33989506::TCTCTCTCTCT… NC_000006.12:33989506::TCTCTCTCTCTCTCTCTCTCTC	NC_000006.12:33989506:TCTCTCTCTCTC… NC_000006.12:33989506:TCTCTCTCTCTCTCTCTCTCTCTC:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC	(self)
1360588916	NC_000006.12:33989506:TCTCTCTCTCTC… NC_000006.12:33989506:TCTCTCTCTCTCTCTCTCTCTCTC:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC	NC_000006.12:33989506:TCTCTCTCTCTC… NC_000006.12:33989506:TCTCTCTCTCTCTCTCTCTCTCTC:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC	(self)
ss4139647076, ss5714840514	NC_000006.12:33989506::TCTCTCTCTCT… NC_000006.12:33989506::TCTCTCTCTCTCTCTCTCTCTCTC	NC_000006.12:33989506:TCTCTCTCTCTC… NC_000006.12:33989506:TCTCTCTCTCTCTCTCTCTCTCTC:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC	(self)
1360588916	NC_000006.12:33989506:TCTCTCTCTCTC… NC_000006.12:33989506:TCTCTCTCTCTCTCTCTCTCTCTC:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC	NC_000006.12:33989506:TCTCTCTCTCTC… NC_000006.12:33989506:TCTCTCTCTCTCTCTCTCTCTCTC:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC	(self)
ss4139647077	NC_000006.12:33989506::TCTCTCTCTCT… NC_000006.12:33989506::TCTCTCTCTCTCTCTCTCTCTCTCTC	NC_000006.12:33989506:TCTCTCTCTCTC… NC_000006.12:33989506:TCTCTCTCTCTCTCTCTCTCTCTC:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC	(self)
1360588916	NC_000006.12:33989506:TCTCTCTCTCTC… NC_000006.12:33989506:TCTCTCTCTCTCTCTCTCTCTCTC:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC	NC_000006.12:33989506:TCTCTCTCTCTC… NC_000006.12:33989506:TCTCTCTCTCTCTCTCTCTCTCTC:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC	(self)
ss4139647078	NC_000006.12:33989506::TCTCTCTCTCT… NC_000006.12:33989506::TCTCTCTCTCTCTCTCTCTCTCTCTCTC	NC_000006.12:33989506:TCTCTCTCTCTC… NC_000006.12:33989506:TCTCTCTCTCTCTCTCTCTCTCTC:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC	(self)
1360588916	NC_000006.12:33989506:TCTCTCTCTCTC… NC_000006.12:33989506:TCTCTCTCTCTCTCTCTCTCTCTC:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC	NC_000006.12:33989506:TCTCTCTCTCTC… NC_000006.12:33989506:TCTCTCTCTCTCTCTCTCTCTCTC:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC	(self)
ss4139647079	NC_000006.12:33989506::TCTCTCTCTCT… NC_000006.12:33989506::TCTCTCTCTCTCTCTCTCTCTCTCTCTCTC	NC_000006.12:33989506:TCTCTCTCTCTC… NC_000006.12:33989506:TCTCTCTCTCTCTCTCTCTCTCTC:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC	(self)
ss4139647080	NC_000006.12:33989506::TCTCTCTCTCT… NC_000006.12:33989506::TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC	NC_000006.12:33989506:TCTCTCTCTCTC… NC_000006.12:33989506:TCTCTCTCTCTCTCTCTCTCTCTC:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC	(self)
ss4139647081	NC_000006.12:33989506::TCTCTCTCTCT… NC_000006.12:33989506::TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC	NC_000006.12:33989506:TCTCTCTCTCTC… NC_000006.12:33989506:TCTCTCTCTCTCTCTCTCTCTCTC:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC	(self)
ss4139647082	NC_000006.12:33989506::TCTCTCTCTCT… NC_000006.12:33989506::TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC	NC_000006.12:33989506:TCTCTCTCTCTC… NC_000006.12:33989506:TCTCTCTCTCTCTCTCTCTCTCTC:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC	(self)
ss4139647083	NC_000006.12:33989506::TCTCTCTCTCT… NC_000006.12:33989506::TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC	NC_000006.12:33989506:TCTCTCTCTCTC… NC_000006.12:33989506:TCTCTCTCTCTCTCTCTCTCTCTC:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC	(self)
ss4139647084	NC_000006.12:33989506::TCTCTCTCTCT… NC_000006.12:33989506::TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC	NC_000006.12:33989506:TCTCTCTCTCTC… NC_000006.12:33989506:TCTCTCTCTCTCTCTCTCTCTCTC:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC	(self)

Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

No publications for rs57445354

The Flanks tab provides retrieving flanking sequences of a SNP on all molecules that have placements.

Genome context:

Select flank length:

Genomic regions, transcripts, and products
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NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs57445354