Name: rs57674095
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.

rs57674095

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr6:2415293-2415307 (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(A)₆ / del(A)₅ / del(A)₄ / delA…
del(A)₆ / del(A)₅ / del(A)₄ / delAAA / delAA / delA / dupA / dupAA / dupAAA / dup(A)₆ / dup(A)₁₄
Variation Type: Indel Insertion and Deletion
Frequency: delAAA=0.4089 (2048/5008, 1000G)
del(A)₄=0.0000 (0/4162, ALFA)
delAAA=0.0000 (0/4162, ALFA) (+ 5 more)
delAA=0.0000 (0/4162, ALFA)
delA=0.0000 (0/4162, ALFA)
dupA=0.0000 (0/4162, ALFA)
dupAA=0.0000 (0/4162, ALFA)
dupAAA=0.0000 (0/4162, 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	4162	AAAAAAAAAAAAAAA=1.0000	AAAAAAAAAAA=0.0000, AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000
European	Sub	3392	AAAAAAAAAAAAAAA=1.0000	AAAAAAAAAAA=0.0000, AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000
African	Sub	450	AAAAAAAAAAAAAAA=1.000	AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000
African Others	Sub	8	AAAAAAAAAAAAAAA=1.0	AAAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0
African American	Sub	442	AAAAAAAAAAAAAAA=1.000	AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000
Asian	Sub	16	AAAAAAAAAAAAAAA=1.00	AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00
East Asian	Sub	10	AAAAAAAAAAAAAAA=1.0	AAAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0
Other Asian	Sub	6	AAAAAAAAAAAAAAA=1.0	AAAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0
Latin American 1	Sub	40	AAAAAAAAAAAAAAA=1.00	AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00
Latin American 2	Sub	96	AAAAAAAAAAAAAAA=1.00	AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00
South Asian	Sub	26	AAAAAAAAAAAAAAA=1.00	AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00
Other	Sub	142	AAAAAAAAAAAAAAA=1.000	AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=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
1000Genomes	Global	Study-wide	5008	(A)₁₅=0.5911	delAAA=0.4089
1000Genomes	African	Sub	1322	(A)₁₅=0.4599	delAAA=0.5401
1000Genomes	East Asian	Sub	1008	(A)₁₅=0.5903	delAAA=0.4097
1000Genomes	Europe	Sub	1006	(A)₁₅=0.7346	delAAA=0.2654
1000Genomes	South Asian	Sub	978	(A)₁₅=0.618	delAAA=0.382
1000Genomes	American	Sub	694	(A)₁₅=0.597	delAAA=0.403
Allele Frequency Aggregator	Total	Global	4162	(A)₁₅=1.0000	del(A)₄=0.0000, delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dupAAA=0.0000
Allele Frequency Aggregator	European	Sub	3392	(A)₁₅=1.0000	del(A)₄=0.0000, delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dupAAA=0.0000
Allele Frequency Aggregator	African	Sub	450	(A)₁₅=1.000	del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000
Allele Frequency Aggregator	Other	Sub	142	(A)₁₅=1.000	del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000
Allele Frequency Aggregator	Latin American 2	Sub	96	(A)₁₅=1.00	del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00
Allele Frequency Aggregator	Latin American 1	Sub	40	(A)₁₅=1.00	del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00
Allele Frequency Aggregator	South Asian	Sub	26	(A)₁₅=1.00	del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00
Allele Frequency Aggregator	Asian	Sub	16	(A)₁₅=1.00	del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=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.2415302_2415307del
GRCh38.p14 chr 6	NC_000006.12:g.2415303_2415307del
GRCh38.p14 chr 6	NC_000006.12:g.2415304_2415307del
GRCh38.p14 chr 6	NC_000006.12:g.2415305_2415307del
GRCh38.p14 chr 6	NC_000006.12:g.2415306_2415307del
GRCh38.p14 chr 6	NC_000006.12:g.2415307del
GRCh38.p14 chr 6	NC_000006.12:g.2415307dup
GRCh38.p14 chr 6	NC_000006.12:g.2415306_2415307dup
GRCh38.p14 chr 6	NC_000006.12:g.2415305_2415307dup
GRCh38.p14 chr 6	NC_000006.12:g.2415302_2415307dup
GRCh38.p14 chr 6	NC_000006.12:g.2415294_2415307dup
GRCh37.p13 chr 6	NC_000006.11:g.2415536_2415541del
GRCh37.p13 chr 6	NC_000006.11:g.2415537_2415541del
GRCh37.p13 chr 6	NC_000006.11:g.2415538_2415541del
GRCh37.p13 chr 6	NC_000006.11:g.2415539_2415541del
GRCh37.p13 chr 6	NC_000006.11:g.2415540_2415541del
GRCh37.p13 chr 6	NC_000006.11:g.2415541del
GRCh37.p13 chr 6	NC_000006.11:g.2415541dup
GRCh37.p13 chr 6	NC_000006.11:g.2415540_2415541dup
GRCh37.p13 chr 6	NC_000006.11:g.2415539_2415541dup
GRCh37.p13 chr 6	NC_000006.11:g.2415536_2415541dup
GRCh37.p13 chr 6	NC_000006.11:g.2415528_2415541dup

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	(A)₁₅=	del(A)₆	del(A)₅	del(A)₄	delAAA	delAA	delA	dupA	dupAA	dupAAA	dup(A)₆	dup(A)₁₄
GRCh38.p14 chr 6	NC_000006.12:g.2415293_2415307=	NC_000006.12:g.2415302_2415307del	NC_000006.12:g.2415303_2415307del	NC_000006.12:g.2415304_2415307del	NC_000006.12:g.2415305_2415307del	NC_000006.12:g.2415306_2415307del	NC_000006.12:g.2415307del	NC_000006.12:g.2415307dup	NC_000006.12:g.2415306_2415307dup	NC_000006.12:g.2415305_2415307dup	NC_000006.12:g.2415302_2415307dup	NC_000006.12:g.2415294_2415307dup
GRCh37.p13 chr 6	NC_000006.11:g.2415527_2415541=	NC_000006.11:g.2415536_2415541del	NC_000006.11:g.2415537_2415541del	NC_000006.11:g.2415538_2415541del	NC_000006.11:g.2415539_2415541del	NC_000006.11:g.2415540_2415541del	NC_000006.11:g.2415541del	NC_000006.11:g.2415541dup	NC_000006.11:g.2415540_2415541dup	NC_000006.11:g.2415539_2415541dup	NC_000006.11:g.2415536_2415541dup	NC_000006.11:g.2415528_2415541dup

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#.

71 SubSNP, 35 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss81785385	Aug 21, 2014 (142)
2	HGSV	ss81851888	Aug 21, 2014 (142)
3	HGSV	ss82328421	Dec 15, 2007 (136)
4	HUMANGENOME_JCVI	ss95417176	Feb 05, 2009 (136)
5	BUSHMAN	ss193841491	Jul 04, 2010 (142)
6	GMI	ss288679355	May 04, 2012 (137)
7	PJP	ss295260817	May 09, 2011 (142)
8	1000GENOMES	ss1375032580	Aug 21, 2014 (142)
9	EVA_UK10K_ALSPAC	ss1705009801	Apr 01, 2015 (144)
10	EVA_UK10K_TWINSUK	ss1705009802	Apr 01, 2015 (144)
11	EVA_UK10K_TWINSUK	ss1710249214	Apr 01, 2015 (144)
12	EVA_UK10K_ALSPAC	ss1710249225	Apr 01, 2015 (144)
13	HAMMER_LAB	ss1804246726	Sep 08, 2015 (146)
14	SWEGEN	ss2998405058	Nov 08, 2017 (151)
15	MCHAISSO	ss3064189181	Nov 08, 2017 (151)
16	MCHAISSO	ss3065065455	Nov 08, 2017 (151)
17	MCHAISSO	ss3065065456	Nov 08, 2017 (151)
18	EVA_DECODE	ss3716446200	Jul 13, 2019 (153)
19	EVA_DECODE	ss3716446201	Jul 13, 2019 (153)
20	EVA_DECODE	ss3716446202	Jul 13, 2019 (153)
21	EVA_DECODE	ss3716446203	Jul 13, 2019 (153)
22	EVA_DECODE	ss3716446204	Jul 13, 2019 (153)
23	EVA_DECODE	ss3716446205	Jul 13, 2019 (153)
24	ACPOP	ss3733141254	Jul 13, 2019 (153)
25	ACPOP	ss3733141255	Jul 13, 2019 (153)
26	ACPOP	ss3733141256	Jul 13, 2019 (153)
27	PACBIO	ss3785352325	Jul 13, 2019 (153)
28	PACBIO	ss3790720569	Jul 13, 2019 (153)
29	PACBIO	ss3795597712	Jul 13, 2019 (153)
30	KHV_HUMAN_GENOMES	ss3807687233	Jul 13, 2019 (153)
31	EVA	ss3829694031	Apr 26, 2020 (154)
32	EVA	ss3838321292	Apr 26, 2020 (154)
33	EVA	ss3843761059	Apr 26, 2020 (154)
34	KOGIC	ss3958366345	Apr 26, 2020 (154)
35	KOGIC	ss3958366346	Apr 26, 2020 (154)
36	KOGIC	ss3958366347	Apr 26, 2020 (154)
37	KOGIC	ss3958366348	Apr 26, 2020 (154)
38	KOGIC	ss3958366349	Apr 26, 2020 (154)
39	GNOMAD	ss4135795499	Apr 26, 2021 (155)
40	GNOMAD	ss4135795500	Apr 26, 2021 (155)
41	GNOMAD	ss4135795501	Apr 26, 2021 (155)
42	GNOMAD	ss4135795502	Apr 26, 2021 (155)
43	GNOMAD	ss4135795503	Apr 26, 2021 (155)
44	GNOMAD	ss4135795504	Apr 26, 2021 (155)
45	GNOMAD	ss4135795505	Apr 26, 2021 (155)
46	GNOMAD	ss4135795506	Apr 26, 2021 (155)
47	GNOMAD	ss4135795507	Apr 26, 2021 (155)
48	GNOMAD	ss4135795508	Apr 26, 2021 (155)
49	TOMMO_GENOMICS	ss5175855067	Apr 26, 2021 (155)
50	TOMMO_GENOMICS	ss5175855068	Apr 26, 2021 (155)
51	TOMMO_GENOMICS	ss5175855069	Apr 26, 2021 (155)
52	TOMMO_GENOMICS	ss5175855070	Apr 26, 2021 (155)
53	TOMMO_GENOMICS	ss5175855071	Apr 26, 2021 (155)
54	1000G_HIGH_COVERAGE	ss5267160464	Oct 13, 2022 (156)
55	1000G_HIGH_COVERAGE	ss5267160465	Oct 13, 2022 (156)
56	1000G_HIGH_COVERAGE	ss5267160466	Oct 13, 2022 (156)
57	1000G_HIGH_COVERAGE	ss5267160467	Oct 13, 2022 (156)
58	1000G_HIGH_COVERAGE	ss5267160468	Oct 13, 2022 (156)
59	HUGCELL_USP	ss5464976713	Oct 13, 2022 (156)
60	HUGCELL_USP	ss5464976714	Oct 13, 2022 (156)
61	HUGCELL_USP	ss5464976715	Oct 13, 2022 (156)
62	HUGCELL_USP	ss5464976716	Oct 13, 2022 (156)
63	HUGCELL_USP	ss5464976717	Oct 13, 2022 (156)
64	TOMMO_GENOMICS	ss5713433083	Oct 13, 2022 (156)
65	TOMMO_GENOMICS	ss5713433084	Oct 13, 2022 (156)
66	TOMMO_GENOMICS	ss5713433085	Oct 13, 2022 (156)
67	TOMMO_GENOMICS	ss5713433086	Oct 13, 2022 (156)
68	TOMMO_GENOMICS	ss5713433087	Oct 13, 2022 (156)
69	EVA	ss5841697279	Oct 13, 2022 (156)
70	EVA	ss5841697280	Oct 13, 2022 (156)
71	EVA	ss5841697281	Oct 13, 2022 (156)
72	1000Genomes	NC_000006.11 - 2415527	Oct 12, 2018 (152)
73	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 16938030 (NC_000006.11:2415527:A: 725/3854) Row 16938031 (NC_000006.11:2415526:AAA: 682/3854)	-	Oct 12, 2018 (152)
74	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 16938030 (NC_000006.11:2415527:A: 725/3854) Row 16938031 (NC_000006.11:2415526:AAA: 682/3854)	-	Oct 12, 2018 (152)
75	gnomAD - Genomes Submission ignored due to conflicting rows: Row 215200697 (NC_000006.12:2415292::A 4973/117842) Row 215200698 (NC_000006.12:2415292::AA 20/117998) Row 215200699 (NC_000006.12:2415292::AAA 3/118002)...	-	Apr 26, 2021 (155)
76	gnomAD - Genomes Submission ignored due to conflicting rows: Row 215200697 (NC_000006.12:2415292::A 4973/117842) Row 215200698 (NC_000006.12:2415292::AA 20/117998) Row 215200699 (NC_000006.12:2415292::AAA 3/118002)...	-	Apr 26, 2021 (155)
77	gnomAD - Genomes Submission ignored due to conflicting rows: Row 215200697 (NC_000006.12:2415292::A 4973/117842) Row 215200698 (NC_000006.12:2415292::AA 20/117998) Row 215200699 (NC_000006.12:2415292::AAA 3/118002)...	-	Apr 26, 2021 (155)
78	gnomAD - Genomes Submission ignored due to conflicting rows: Row 215200697 (NC_000006.12:2415292::A 4973/117842) Row 215200698 (NC_000006.12:2415292::AA 20/117998) Row 215200699 (NC_000006.12:2415292::AAA 3/118002)...	-	Apr 26, 2021 (155)
79	gnomAD - Genomes Submission ignored due to conflicting rows: Row 215200697 (NC_000006.12:2415292::A 4973/117842) Row 215200698 (NC_000006.12:2415292::AA 20/117998) Row 215200699 (NC_000006.12:2415292::AAA 3/118002)...	-	Apr 26, 2021 (155)
80	gnomAD - Genomes Submission ignored due to conflicting rows: Row 215200697 (NC_000006.12:2415292::A 4973/117842) Row 215200698 (NC_000006.12:2415292::AA 20/117998) Row 215200699 (NC_000006.12:2415292::AAA 3/118002)...	-	Apr 26, 2021 (155)
81	gnomAD - Genomes Submission ignored due to conflicting rows: Row 215200697 (NC_000006.12:2415292::A 4973/117842) Row 215200698 (NC_000006.12:2415292::AA 20/117998) Row 215200699 (NC_000006.12:2415292::AAA 3/118002)...	-	Apr 26, 2021 (155)
82	gnomAD - Genomes Submission ignored due to conflicting rows: Row 215200697 (NC_000006.12:2415292::A 4973/117842) Row 215200698 (NC_000006.12:2415292::AA 20/117998) Row 215200699 (NC_000006.12:2415292::AAA 3/118002)...	-	Apr 26, 2021 (155)
83	gnomAD - Genomes Submission ignored due to conflicting rows: Row 215200697 (NC_000006.12:2415292::A 4973/117842) Row 215200698 (NC_000006.12:2415292::AA 20/117998) Row 215200699 (NC_000006.12:2415292::AAA 3/118002)...	-	Apr 26, 2021 (155)
84	gnomAD - Genomes Submission ignored due to conflicting rows: Row 215200697 (NC_000006.12:2415292::A 4973/117842) Row 215200698 (NC_000006.12:2415292::AA 20/117998) Row 215200699 (NC_000006.12:2415292::AAA 3/118002)...	-	Apr 26, 2021 (155)
85	gnomAD - Genomes Submission ignored due to conflicting rows: Row 215200697 (NC_000006.12:2415292::A 4973/117842) Row 215200698 (NC_000006.12:2415292::AA 20/117998) Row 215200699 (NC_000006.12:2415292::AAA 3/118002)...	-	Apr 26, 2021 (155)
86	Korean Genome Project Submission ignored due to conflicting rows: Row 14744346 (NC_000006.12:2415293:AAA: 341/1830) Row 14744347 (NC_000006.12:2415294:AA: 794/1830) Row 14744348 (NC_000006.12:2415296::A 21/1830)...	-	Apr 26, 2020 (154)
87	Korean Genome Project Submission ignored due to conflicting rows: Row 14744346 (NC_000006.12:2415293:AAA: 341/1830) Row 14744347 (NC_000006.12:2415294:AA: 794/1830) Row 14744348 (NC_000006.12:2415296::A 21/1830)...	-	Apr 26, 2020 (154)
88	Korean Genome Project Submission ignored due to conflicting rows: Row 14744346 (NC_000006.12:2415293:AAA: 341/1830) Row 14744347 (NC_000006.12:2415294:AA: 794/1830) Row 14744348 (NC_000006.12:2415296::A 21/1830)...	-	Apr 26, 2020 (154)
89	Korean Genome Project Submission ignored due to conflicting rows: Row 14744346 (NC_000006.12:2415293:AAA: 341/1830) Row 14744347 (NC_000006.12:2415294:AA: 794/1830) Row 14744348 (NC_000006.12:2415296::A 21/1830)...	-	Apr 26, 2020 (154)
90	Korean Genome Project Submission ignored due to conflicting rows: Row 14744346 (NC_000006.12:2415293:AAA: 341/1830) Row 14744347 (NC_000006.12:2415294:AA: 794/1830) Row 14744348 (NC_000006.12:2415296::A 21/1830)...	-	Apr 26, 2020 (154)
91	Northern Sweden Submission ignored due to conflicting rows: Row 6426119 (NC_000006.11:2415526:AAA: 84/520) Row 6426120 (NC_000006.11:2415526:AA: 82/520) Row 6426121 (NC_000006.11:2415526:AAAA: 3/520)	-	Jul 13, 2019 (153)
92	Northern Sweden Submission ignored due to conflicting rows: Row 6426119 (NC_000006.11:2415526:AAA: 84/520) Row 6426120 (NC_000006.11:2415526:AA: 82/520) Row 6426121 (NC_000006.11:2415526:AAAA: 3/520)	-	Jul 13, 2019 (153)
93	Northern Sweden Submission ignored due to conflicting rows: Row 6426119 (NC_000006.11:2415526:AAA: 84/520) Row 6426120 (NC_000006.11:2415526:AA: 82/520) Row 6426121 (NC_000006.11:2415526:AAAA: 3/520)	-	Jul 13, 2019 (153)
94	8.3KJPN Submission ignored due to conflicting rows: Row 33824374 (NC_000006.11:2415526:AA: 6998/16760) Row 33824375 (NC_000006.11:2415526:AAA: 3165/16760) Row 33824376 (NC_000006.11:2415526:A: 5/16760)...	-	Apr 26, 2021 (155)
95	8.3KJPN Submission ignored due to conflicting rows: Row 33824374 (NC_000006.11:2415526:AA: 6998/16760) Row 33824375 (NC_000006.11:2415526:AAA: 3165/16760) Row 33824376 (NC_000006.11:2415526:A: 5/16760)...	-	Apr 26, 2021 (155)
96	8.3KJPN Submission ignored due to conflicting rows: Row 33824374 (NC_000006.11:2415526:AA: 6998/16760) Row 33824375 (NC_000006.11:2415526:AAA: 3165/16760) Row 33824376 (NC_000006.11:2415526:A: 5/16760)...	-	Apr 26, 2021 (155)
97	8.3KJPN Submission ignored due to conflicting rows: Row 33824374 (NC_000006.11:2415526:AA: 6998/16760) Row 33824375 (NC_000006.11:2415526:AAA: 3165/16760) Row 33824376 (NC_000006.11:2415526:A: 5/16760)...	-	Apr 26, 2021 (155)
98	8.3KJPN Submission ignored due to conflicting rows: Row 33824374 (NC_000006.11:2415526:AA: 6998/16760) Row 33824375 (NC_000006.11:2415526:AAA: 3165/16760) Row 33824376 (NC_000006.11:2415526:A: 5/16760)...	-	Apr 26, 2021 (155)
99	14KJPN Submission ignored due to conflicting rows: Row 47270187 (NC_000006.12:2415292:AA: 11718/28256) Row 47270188 (NC_000006.12:2415292:AAAA: 13/28256) Row 47270189 (NC_000006.12:2415292:AAA: 5426/28256)...	-	Oct 13, 2022 (156)
100	14KJPN Submission ignored due to conflicting rows: Row 47270187 (NC_000006.12:2415292:AA: 11718/28256) Row 47270188 (NC_000006.12:2415292:AAAA: 13/28256) Row 47270189 (NC_000006.12:2415292:AAA: 5426/28256)...	-	Oct 13, 2022 (156)
101	14KJPN Submission ignored due to conflicting rows: Row 47270187 (NC_000006.12:2415292:AA: 11718/28256) Row 47270188 (NC_000006.12:2415292:AAAA: 13/28256) Row 47270189 (NC_000006.12:2415292:AAA: 5426/28256)...	-	Oct 13, 2022 (156)
102	14KJPN Submission ignored due to conflicting rows: Row 47270187 (NC_000006.12:2415292:AA: 11718/28256) Row 47270188 (NC_000006.12:2415292:AAAA: 13/28256) Row 47270189 (NC_000006.12:2415292:AAA: 5426/28256)...	-	Oct 13, 2022 (156)
103	14KJPN Submission ignored due to conflicting rows: Row 47270187 (NC_000006.12:2415292:AA: 11718/28256) Row 47270188 (NC_000006.12:2415292:AAAA: 13/28256) Row 47270189 (NC_000006.12:2415292:AAA: 5426/28256)...	-	Oct 13, 2022 (156)
104	UK 10K study - Twins Submission ignored due to conflicting rows: Row 16938030 (NC_000006.11:2415527:A: 697/3708) Row 16938031 (NC_000006.11:2415526:AAA: 598/3708)	-	Oct 12, 2018 (152)
105	UK 10K study - Twins Submission ignored due to conflicting rows: Row 16938030 (NC_000006.11:2415527:A: 697/3708) Row 16938031 (NC_000006.11:2415526:AAA: 598/3708)	-	Oct 12, 2018 (152)
106	ALFA	NC_000006.12 - 2415293	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)
rs59734739	Oct 14, 2011 (136)
rs112149163	Aug 21, 2014 (142)
rs148962759	Apr 25, 2013 (138)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4135795508	NC_000006.12:2415292:AAAAAA:	NC_000006.12:2415292:AAAAAAAAAAAAA… NC_000006.12:2415292:AAAAAAAAAAAAAAA:AAAAAAAAA	(self)
ss4135795507, ss5464976717	NC_000006.12:2415292:AAAAA:	NC_000006.12:2415292:AAAAAAAAAAAAA… NC_000006.12:2415292:AAAAAAAAAAAAAAA:AAAAAAAAAA	(self)
ss2998405058, ss3733141256, ss5175855070, ss5841697281	NC_000006.11:2415526:AAAA:	NC_000006.12:2415292:AAAAAAAAAAAAA… NC_000006.12:2415292:AAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
ss3716446205, ss3958366348, ss4135795506, ss5267160467, ss5464976716, ss5713433084	NC_000006.12:2415292:AAAA:	NC_000006.12:2415292:AAAAAAAAAAAAA… NC_000006.12:2415292:AAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
7959809124	NC_000006.12:2415292:AAAAAAAAAAAAA… NC_000006.12:2415292:AAAAAAAAAAAAAAA:AAAAAAAAAAA	NC_000006.12:2415292:AAAAAAAAAAAAA… NC_000006.12:2415292:AAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
ss82328421	NC_000006.9:2360537:AAA:	NC_000006.12:2415292:AAAAAAAAAAAAA… NC_000006.12:2415292:AAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss295260817	NC_000006.10:2360537:AAA:	NC_000006.12:2415292:AAAAAAAAAAAAA… NC_000006.12:2415292:AAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
30432165, ss1375032580, ss1705009801, ss1705009802, ss1804246726, ss3733141254, ss5175855068, ss5841697279	NC_000006.11:2415526:AAA:	NC_000006.12:2415292:AAAAAAAAAAAAA… NC_000006.12:2415292:AAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss3064189181, ss3065065455, ss3065065456, ss3807687233, ss4135795505, ss5267160465, ss5464976713, ss5713433085	NC_000006.12:2415292:AAA:	NC_000006.12:2415292:AAAAAAAAAAAAA… NC_000006.12:2415292:AAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
7959809124	NC_000006.12:2415292:AAAAAAAAAAAAA… NC_000006.12:2415292:AAAAAAAAAAAAAAA:AAAAAAAAAAAA	NC_000006.12:2415292:AAAAAAAAAAAAA… NC_000006.12:2415292:AAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss3716446204, ss3958366345	NC_000006.12:2415293:AAA:	NC_000006.12:2415292:AAAAAAAAAAAAA… NC_000006.12:2415292:AAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss95417176	NT_007592.15:2355538:AAA:	NC_000006.12:2415292:AAAAAAAAAAAAA… NC_000006.12:2415292:AAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss193841491	NT_007592.16:2355292:AAA:	NC_000006.12:2415292:AAAAAAAAAAAAA… NC_000006.12:2415292:AAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss81785385, ss81851888	NC_000006.9:2360538:AA:	NC_000006.12:2415292:AAAAAAAAAAAAA… NC_000006.12:2415292:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss288679355	NC_000006.10:2360525:AA:	NC_000006.12:2415292:AAAAAAAAAAAAA… NC_000006.12:2415292:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss3733141255, ss3785352325, ss3790720569, ss3795597712, ss3829694031, ss3838321292, ss5175855067, ss5841697280	NC_000006.11:2415526:AA:	NC_000006.12:2415292:AAAAAAAAAAAAA… NC_000006.12:2415292:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss1710249214, ss1710249225	NC_000006.11:2415527:AA:	NC_000006.12:2415292:AAAAAAAAAAAAA… NC_000006.12:2415292:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss3843761059, ss4135795504, ss5267160464, ss5464976714, ss5713433083	NC_000006.12:2415292:AA:	NC_000006.12:2415292:AAAAAAAAAAAAA… NC_000006.12:2415292:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
7959809124	NC_000006.12:2415292:AAAAAAAAAAAAA… NC_000006.12:2415292:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA	NC_000006.12:2415292:AAAAAAAAAAAAA… NC_000006.12:2415292:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss3716446203, ss3958366346	NC_000006.12:2415294:AA:	NC_000006.12:2415292:AAAAAAAAAAAAA… NC_000006.12:2415292:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss5175855069	NC_000006.11:2415526:A:	NC_000006.12:2415292:AAAAAAAAAAAAA… NC_000006.12:2415292:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
	NC_000006.11:2415527:A:	NC_000006.12:2415292:AAAAAAAAAAAAA… NC_000006.12:2415292:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss5267160468, ss5713433086	NC_000006.12:2415292:A:	NC_000006.12:2415292:AAAAAAAAAAAAA… NC_000006.12:2415292:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
7959809124	NC_000006.12:2415292:AAAAAAAAAAAAA… NC_000006.12:2415292:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000006.12:2415292:AAAAAAAAAAAAA… NC_000006.12:2415292:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss3716446202, ss3958366349	NC_000006.12:2415295:A:	NC_000006.12:2415292:AAAAAAAAAAAAA… NC_000006.12:2415292:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss5175855071	NC_000006.11:2415526::A	NC_000006.12:2415292:AAAAAAAAAAAAA… NC_000006.12:2415292:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss4135795499, ss5267160466, ss5464976715, ss5713433087	NC_000006.12:2415292::A	NC_000006.12:2415292:AAAAAAAAAAAAA… NC_000006.12:2415292:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
7959809124	NC_000006.12:2415292:AAAAAAAAAAAAA… NC_000006.12:2415292:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000006.12:2415292:AAAAAAAAAAAAA… NC_000006.12:2415292:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss3716446201, ss3958366347	NC_000006.12:2415296::A	NC_000006.12:2415292:AAAAAAAAAAAAA… NC_000006.12:2415292:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss4135795500	NC_000006.12:2415292::AA	NC_000006.12:2415292:AAAAAAAAAAAAA… NC_000006.12:2415292:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
7959809124	NC_000006.12:2415292:AAAAAAAAAAAAA… NC_000006.12:2415292:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000006.12:2415292:AAAAAAAAAAAAA… NC_000006.12:2415292:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss4135795501	NC_000006.12:2415292::AAA	NC_000006.12:2415292:AAAAAAAAAAAAA… NC_000006.12:2415292:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
7959809124	NC_000006.12:2415292:AAAAAAAAAAAAA… NC_000006.12:2415292:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000006.12:2415292:AAAAAAAAAAAAA… NC_000006.12:2415292:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss3716446200	NC_000006.12:2415296::AAA	NC_000006.12:2415292:AAAAAAAAAAAAA… NC_000006.12:2415292:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss4135795502	NC_000006.12:2415292::AAAAAA	NC_000006.12:2415292:AAAAAAAAAAAAA… NC_000006.12:2415292:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss4135795503	NC_000006.12:2415292::AAAAAAAAAAAA… NC_000006.12:2415292::AAAAAAAAAAAAAA	NC_000006.12:2415292:AAAAAAAAAAAAA… NC_000006.12:2415292:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(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 rs57674095

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
Top▲ Help
NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
Use the zoom option to view the nucleotides around the RefSNP and find other neighboring RefSNPs.
Visit Sequence Viewer for help with navigating inside the display and modifying the selection of displayed data tracks.

Choose placement

dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs57674095