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dbSNP Short Genetic Variations

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.

rs2053724

Current Build 155

Released April 9, 2021

Organism
Homo sapiens
Position
chr2:115753241 (GRCh38.p13) 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
G>A / G>C / G>T
Variation Type
SNV Single Nucleotide Variation
Frequency
C=0.499981 (132340/264690, TOPMED)
G=0.389236 (47124/121068, ExAC)
G=0.44214 (17966/40634, ALFA) (+ 18 more)
G=0.26993 (4524/16760, 8.3KJPN)
C=0.47801 (6217/13006, GO-ESP)
G=0.4706 (2357/5008, 1000G)
G=0.3190 (1429/4480, Estonian)
G=0.3936 (1517/3854, ALSPAC)
G=0.3889 (1442/3708, TWINSUK)
G=0.3014 (883/2930, KOREAN)
G=0.416 (415/998, GoNL)
G=0.295 (233/790, PRJEB37584)
G=0.242 (148/611, Vietnamese)
G=0.332 (199/600, NorthernSweden)
G=0.395 (211/534, MGP)
G=0.265 (114/430, SGDP_PRJ)
C=0.469 (152/324, HapMap)
G=0.224 (68/304, FINRISK)
C=0.407 (88/216, Qatari)
G=0.37 (20/54, Siberian)
G=0.40 (16/40, GENOME_DK)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
DPP10 : Missense Variant
LOC105373572 : Intron Variant
Publications
1 citation
Genomic View
See rs on genome
Help

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.p13 chr 2 NC_000002.12:g.115753241G>A
GRCh38.p13 chr 2 NC_000002.12:g.115753241G>C
GRCh38.p13 chr 2 NC_000002.12:g.115753241G>T
GRCh37.p13 chr 2 NC_000002.11:g.116510817G>A
GRCh37.p13 chr 2 NC_000002.11:g.116510817G>C
GRCh37.p13 chr 2 NC_000002.11:g.116510817G>T
Gene: DPP10, dipeptidyl peptidase like 10 (plus strand)
Molecule type Change Amino acid[Codon] SO Term
DPP10 transcript variant 3 NM_001178034.1:c.1030G>A A [GCT] > T [ACT] Coding Sequence Variant
inactive dipeptidyl peptidase 10 isoform c NP_001171505.1:p.Ala344Thr A (Ala) > T (Thr) Missense Variant
DPP10 transcript variant 3 NM_001178034.1:c.1030G>C A [GCT] > P [CCT] Coding Sequence Variant
inactive dipeptidyl peptidase 10 isoform c NP_001171505.1:p.Ala344Pro A (Ala) > P (Pro) Missense Variant
DPP10 transcript variant 3 NM_001178034.1:c.1030G>T A [GCT] > S [TCT] Coding Sequence Variant
inactive dipeptidyl peptidase 10 isoform c NP_001171505.1:p.Ala344Ser A (Ala) > S (Ser) Missense Variant
DPP10 transcript variant 1 NM_020868.6:c.1018G>A A [GCT] > T [ACT] Coding Sequence Variant
inactive dipeptidyl peptidase 10 isoform long NP_065919.3:p.Ala340Thr A (Ala) > T (Thr) Missense Variant
DPP10 transcript variant 1 NM_020868.6:c.1018G>C A [GCT] > P [CCT] Coding Sequence Variant
inactive dipeptidyl peptidase 10 isoform long NP_065919.3:p.Ala340Pro A (Ala) > P (Pro) Missense Variant
DPP10 transcript variant 1 NM_020868.6:c.1018G>T A [GCT] > S [TCT] Coding Sequence Variant
inactive dipeptidyl peptidase 10 isoform long NP_065919.3:p.Ala340Ser A (Ala) > S (Ser) Missense Variant
DPP10 transcript variant 7 NM_001321906.2:c.997G>A A [GCT] > T [ACT] Coding Sequence Variant
inactive dipeptidyl peptidase 10 isoform short NP_001308835.2:p.Ala333Thr A (Ala) > T (Thr) Missense Variant
DPP10 transcript variant 7 NM_001321906.2:c.997G>C A [GCT] > P [CCT] Coding Sequence Variant
inactive dipeptidyl peptidase 10 isoform short NP_001308835.2:p.Ala333Pro A (Ala) > P (Pro) Missense Variant
DPP10 transcript variant 7 NM_001321906.2:c.997G>T A [GCT] > S [TCT] Coding Sequence Variant
inactive dipeptidyl peptidase 10 isoform short NP_001308835.2:p.Ala333Ser A (Ala) > S (Ser) Missense Variant
DPP10 transcript variant 15 NM_001321914.2:c.256G>A A [GCT] > T [ACT] Coding Sequence Variant
inactive dipeptidyl peptidase 10 isoform i NP_001308843.2:p.Ala86Thr A (Ala) > T (Thr) Missense Variant
DPP10 transcript variant 15 NM_001321914.2:c.256G>C A [GCT] > P [CCT] Coding Sequence Variant
inactive dipeptidyl peptidase 10 isoform i NP_001308843.2:p.Ala86Pro A (Ala) > P (Pro) Missense Variant
DPP10 transcript variant 15 NM_001321914.2:c.256G>T A [GCT] > S [TCT] Coding Sequence Variant
inactive dipeptidyl peptidase 10 isoform i NP_001308843.2:p.Ala86Ser A (Ala) > S (Ser) Missense Variant
DPP10 transcript variant 9 NM_001321908.3:c.928G>A A [GCT] > T [ACT] Coding Sequence Variant
inactive dipeptidyl peptidase 10 isoform f NP_001308837.2:p.Ala310Thr A (Ala) > T (Thr) Missense Variant
DPP10 transcript variant 9 NM_001321908.3:c.928G>C A [GCT] > P [CCT] Coding Sequence Variant
inactive dipeptidyl peptidase 10 isoform f NP_001308837.2:p.Ala310Pro A (Ala) > P (Pro) Missense Variant
DPP10 transcript variant 9 NM_001321908.3:c.928G>T A [GCT] > S [TCT] Coding Sequence Variant
inactive dipeptidyl peptidase 10 isoform f NP_001308837.2:p.Ala310Ser A (Ala) > S (Ser) Missense Variant
DPP10 transcript variant 5 NM_001178036.3:c.868G>A A [GCT] > T [ACT] Coding Sequence Variant
inactive dipeptidyl peptidase 10 isoform a NP_001171507.2:p.Ala290Thr A (Ala) > T (Thr) Missense Variant
DPP10 transcript variant 5 NM_001178036.3:c.868G>C A [GCT] > P [CCT] Coding Sequence Variant
inactive dipeptidyl peptidase 10 isoform a NP_001171507.2:p.Ala290Pro A (Ala) > P (Pro) Missense Variant
DPP10 transcript variant 5 NM_001178036.3:c.868G>T A [GCT] > S [TCT] Coding Sequence Variant
inactive dipeptidyl peptidase 10 isoform a NP_001171507.2:p.Ala290Ser A (Ala) > S (Ser) Missense Variant
DPP10 transcript variant 4 NM_001178037.3:c.1006G>A A [GCT] > T [ACT] Coding Sequence Variant
inactive dipeptidyl peptidase 10 isoform b NP_001171508.2:p.Ala336Thr A (Ala) > T (Thr) Missense Variant
DPP10 transcript variant 4 NM_001178037.3:c.1006G>C A [GCT] > P [CCT] Coding Sequence Variant
inactive dipeptidyl peptidase 10 isoform b NP_001171508.2:p.Ala336Pro A (Ala) > P (Pro) Missense Variant
DPP10 transcript variant 4 NM_001178037.3:c.1006G>T A [GCT] > S [TCT] Coding Sequence Variant
inactive dipeptidyl peptidase 10 isoform b NP_001171508.2:p.Ala336Ser A (Ala) > S (Ser) Missense Variant
DPP10 transcript variant 13 NM_001321912.3:c.868G>A A [GCT] > T [ACT] Coding Sequence Variant
inactive dipeptidyl peptidase 10 isoform h NP_001308841.2:p.Ala290Thr A (Ala) > T (Thr) Missense Variant
DPP10 transcript variant 13 NM_001321912.3:c.868G>C A [GCT] > P [CCT] Coding Sequence Variant
inactive dipeptidyl peptidase 10 isoform h NP_001308841.2:p.Ala290Pro A (Ala) > P (Pro) Missense Variant
DPP10 transcript variant 13 NM_001321912.3:c.868G>T A [GCT] > S [TCT] Coding Sequence Variant
inactive dipeptidyl peptidase 10 isoform h NP_001308841.2:p.Ala290Ser A (Ala) > S (Ser) Missense Variant
DPP10 transcript variant 8 NM_001321907.3:c.1018G>A A [GCT] > T [ACT] Coding Sequence Variant
inactive dipeptidyl peptidase 10 isoform e NP_001308836.2:p.Ala340Thr A (Ala) > T (Thr) Missense Variant
DPP10 transcript variant 8 NM_001321907.3:c.1018G>C A [GCT] > P [CCT] Coding Sequence Variant
inactive dipeptidyl peptidase 10 isoform e NP_001308836.2:p.Ala340Pro A (Ala) > P (Pro) Missense Variant
DPP10 transcript variant 8 NM_001321907.3:c.1018G>T A [GCT] > S [TCT] Coding Sequence Variant
inactive dipeptidyl peptidase 10 isoform e NP_001308836.2:p.Ala340Ser A (Ala) > S (Ser) Missense Variant
DPP10 transcript variant 6 NM_001321905.3:c.1069G>A A [GCT] > T [ACT] Coding Sequence Variant
inactive dipeptidyl peptidase 10 isoform d NP_001308834.2:p.Ala357Thr A (Ala) > T (Thr) Missense Variant
DPP10 transcript variant 6 NM_001321905.3:c.1069G>C A [GCT] > P [CCT] Coding Sequence Variant
inactive dipeptidyl peptidase 10 isoform d NP_001308834.2:p.Ala357Pro A (Ala) > P (Pro) Missense Variant
DPP10 transcript variant 6 NM_001321905.3:c.1069G>T A [GCT] > S [TCT] Coding Sequence Variant
inactive dipeptidyl peptidase 10 isoform d NP_001308834.2:p.Ala357Ser A (Ala) > S (Ser) Missense Variant
DPP10 transcript variant 10 NM_001321909.3:c.901G>A A [GCT] > T [ACT] Coding Sequence Variant
inactive dipeptidyl peptidase 10 isoform g NP_001308838.2:p.Ala301Thr A (Ala) > T (Thr) Missense Variant
DPP10 transcript variant 10 NM_001321909.3:c.901G>C A [GCT] > P [CCT] Coding Sequence Variant
inactive dipeptidyl peptidase 10 isoform g NP_001308838.2:p.Ala301Pro A (Ala) > P (Pro) Missense Variant
DPP10 transcript variant 10 NM_001321909.3:c.901G>T A [GCT] > S [TCT] Coding Sequence Variant
inactive dipeptidyl peptidase 10 isoform g NP_001308838.2:p.Ala301Ser A (Ala) > S (Ser) Missense Variant
DPP10 transcript variant 2 NM_001004360.5:c.997G>A A [GCT] > T [ACT] Coding Sequence Variant
inactive dipeptidyl peptidase 10 isoform short NP_001004360.3:p.Ala333Thr A (Ala) > T (Thr) Missense Variant
DPP10 transcript variant 2 NM_001004360.5:c.997G>C A [GCT] > P [CCT] Coding Sequence Variant
inactive dipeptidyl peptidase 10 isoform short NP_001004360.3:p.Ala333Pro A (Ala) > P (Pro) Missense Variant
DPP10 transcript variant 2 NM_001004360.5:c.997G>T A [GCT] > S [TCT] Coding Sequence Variant
inactive dipeptidyl peptidase 10 isoform short NP_001004360.3:p.Ala333Ser A (Ala) > S (Ser) Missense Variant
DPP10 transcript variant 14 NM_001321913.3:c.256G>A A [GCT] > T [ACT] Coding Sequence Variant
inactive dipeptidyl peptidase 10 isoform i NP_001308842.2:p.Ala86Thr A (Ala) > T (Thr) Missense Variant
DPP10 transcript variant 14 NM_001321913.3:c.256G>C A [GCT] > P [CCT] Coding Sequence Variant
inactive dipeptidyl peptidase 10 isoform i NP_001308842.2:p.Ala86Pro A (Ala) > P (Pro) Missense Variant
DPP10 transcript variant 14 NM_001321913.3:c.256G>T A [GCT] > S [TCT] Coding Sequence Variant
inactive dipeptidyl peptidase 10 isoform i NP_001308842.2:p.Ala86Ser A (Ala) > S (Ser) Missense Variant
DPP10 transcript variant 11 NM_001321910.3:c.868G>A A [GCT] > T [ACT] Coding Sequence Variant
inactive dipeptidyl peptidase 10 isoform a NP_001308839.2:p.Ala290Thr A (Ala) > T (Thr) Missense Variant
DPP10 transcript variant 11 NM_001321910.3:c.868G>C A [GCT] > P [CCT] Coding Sequence Variant
inactive dipeptidyl peptidase 10 isoform a NP_001308839.2:p.Ala290Pro A (Ala) > P (Pro) Missense Variant
DPP10 transcript variant 11 NM_001321910.3:c.868G>T A [GCT] > S [TCT] Coding Sequence Variant
inactive dipeptidyl peptidase 10 isoform a NP_001308839.2:p.Ala290Ser A (Ala) > S (Ser) Missense Variant
DPP10 transcript variant 12 NM_001321911.3:c.868G>A A [GCT] > T [ACT] Coding Sequence Variant
inactive dipeptidyl peptidase 10 isoform a NP_001308840.2:p.Ala290Thr A (Ala) > T (Thr) Missense Variant
DPP10 transcript variant 12 NM_001321911.3:c.868G>C A [GCT] > P [CCT] Coding Sequence Variant
inactive dipeptidyl peptidase 10 isoform a NP_001308840.2:p.Ala290Pro A (Ala) > P (Pro) Missense Variant
DPP10 transcript variant 12 NM_001321911.3:c.868G>T A [GCT] > S [TCT] Coding Sequence Variant
inactive dipeptidyl peptidase 10 isoform a NP_001308840.2:p.Ala290Ser A (Ala) > S (Ser) Missense Variant
DPP10 transcript variant X2 XM_017004566.1:c.895G>A A [GCT] > T [ACT] Coding Sequence Variant
inactive dipeptidyl peptidase 10 isoform X2 XP_016860055.1:p.Ala299Thr A (Ala) > T (Thr) Missense Variant
DPP10 transcript variant X2 XM_017004566.1:c.895G>C A [GCT] > P [CCT] Coding Sequence Variant
inactive dipeptidyl peptidase 10 isoform X2 XP_016860055.1:p.Ala299Pro A (Ala) > P (Pro) Missense Variant
DPP10 transcript variant X2 XM_017004566.1:c.895G>T A [GCT] > S [TCT] Coding Sequence Variant
inactive dipeptidyl peptidase 10 isoform X2 XP_016860055.1:p.Ala299Ser A (Ala) > S (Ser) Missense Variant
DPP10 transcript variant X1 XM_024453023.1:c.997G>A A [GCT] > T [ACT] Coding Sequence Variant
inactive dipeptidyl peptidase 10 isoform X1 XP_024308791.1:p.Ala333Thr A (Ala) > T (Thr) Missense Variant
DPP10 transcript variant X1 XM_024453023.1:c.997G>C A [GCT] > P [CCT] Coding Sequence Variant
inactive dipeptidyl peptidase 10 isoform X1 XP_024308791.1:p.Ala333Pro A (Ala) > P (Pro) Missense Variant
DPP10 transcript variant X1 XM_024453023.1:c.997G>T A [GCT] > S [TCT] Coding Sequence Variant
inactive dipeptidyl peptidase 10 isoform X1 XP_024308791.1:p.Ala333Ser A (Ala) > S (Ser) Missense Variant
Gene: LOC105373572, uncharacterized LOC105373572 (minus strand)
Molecule type Change Amino acid[Codon] SO Term
LOC105373572 transcript XR_923234.2:n. N/A Intron Variant
Help

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

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: 20201027095038
Population Group Sample Size Ref Allele Alt Allele
Total Global 40634 G=0.44214 A=0.00000, C=0.55786
European Sub 30864 G=0.40944 A=0.00000, C=0.59056
African Sub 2518 G=0.8797 A=0.0000, C=0.1203
African Others Sub 96 G=0.98 A=0.00, C=0.02
African American Sub 2422 G=0.8757 A=0.0000, C=0.1243
Asian Sub 68 G=0.35 A=0.00, C=0.65
East Asian Sub 36 G=0.47 A=0.00, C=0.53
Other Asian Sub 32 G=0.22 A=0.00, C=0.78
Latin American 1 Sub 390 G=0.574 A=0.000, C=0.426
Latin American 2 Sub 62 G=0.85 A=0.00, C=0.15
South Asian Sub 18 G=0.89 A=0.00, C=0.11
Other Sub 6714 G=0.4166 A=0.0000, C=0.5834


Help

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
TopMed Global Study-wide 264690 G=0.500019 C=0.499981
ExAC Global Study-wide 121068 G=0.389236 C=0.610764
ExAC Europe Sub 73176 G=0.37018 C=0.62982
ExAC Asian Sub 25082 G=0.36520 C=0.63480
ExAC American Sub 11514 G=0.21096 C=0.78904
ExAC African Sub 10390 G=0.77950 C=0.22050
ExAC Other Sub 906 G=0.384 C=0.616
Allele Frequency Aggregator Total Global 40634 G=0.44214 A=0.00000, C=0.55786
Allele Frequency Aggregator European Sub 30864 G=0.40944 A=0.00000, C=0.59056
Allele Frequency Aggregator Other Sub 6714 G=0.4166 A=0.0000, C=0.5834
Allele Frequency Aggregator African Sub 2518 G=0.8797 A=0.0000, C=0.1203
Allele Frequency Aggregator Latin American 1 Sub 390 G=0.574 A=0.000, C=0.426
Allele Frequency Aggregator Asian Sub 68 G=0.35 A=0.00, C=0.65
Allele Frequency Aggregator Latin American 2 Sub 62 G=0.85 A=0.00, C=0.15
Allele Frequency Aggregator South Asian Sub 18 G=0.89 A=0.00, C=0.11
8.3KJPN JAPANESE Study-wide 16760 G=0.26993 C=0.73007
GO Exome Sequencing Project Global Study-wide 13006 G=0.52199 C=0.47801
GO Exome Sequencing Project European American Sub 8600 G=0.3935 C=0.6065
GO Exome Sequencing Project African American Sub 4406 G=0.7728 C=0.2272
1000Genomes Global Study-wide 5008 G=0.4706 C=0.5294
1000Genomes African Sub 1322 G=0.8411 C=0.1589
1000Genomes East Asian Sub 1008 G=0.2679 C=0.7321
1000Genomes Europe Sub 1006 G=0.3748 C=0.6252
1000Genomes South Asian Sub 978 G=0.421 C=0.579
1000Genomes American Sub 694 G=0.268 C=0.732
Genetic variation in the Estonian population Estonian Study-wide 4480 G=0.3190 C=0.6810
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 G=0.3936 C=0.6064
UK 10K study - Twins TWIN COHORT Study-wide 3708 G=0.3889 C=0.6111
KOREAN population from KRGDB KOREAN Study-wide 2930 G=0.3014 C=0.6986, T=0.0000
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 G=0.416 C=0.584
CNV burdens in cranial meningiomas Global Study-wide 790 G=0.295 C=0.705
CNV burdens in cranial meningiomas CRM Sub 790 G=0.295 C=0.705
A Vietnamese Genetic Variation Database Global Study-wide 611 G=0.242 C=0.758
Northern Sweden ACPOP Study-wide 600 G=0.332 C=0.668
Medical Genome Project healthy controls from Spanish population Spanish controls Study-wide 534 G=0.395 C=0.605
SGDP_PRJ Global Study-wide 430 G=0.265 C=0.735
HapMap Global Study-wide 324 G=0.531 C=0.469
HapMap African Sub 118 G=0.898 C=0.102
HapMap American Sub 118 G=0.364 C=0.636
HapMap Asian Sub 88 G=0.26 C=0.74
FINRISK Finnish from FINRISK project Study-wide 304 G=0.224 C=0.776
Qatari Global Study-wide 216 G=0.593 C=0.407
Siberian Global Study-wide 54 G=0.37 C=0.63
The Danish reference pan genome Danish Study-wide 40 G=0.40 C=0.60
Help

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 G= A C T
GRCh38.p13 chr 2 NC_000002.12:g.115753241= NC_000002.12:g.115753241G>A NC_000002.12:g.115753241G>C NC_000002.12:g.115753241G>T
GRCh37.p13 chr 2 NC_000002.11:g.116510817= NC_000002.11:g.116510817G>A NC_000002.11:g.116510817G>C NC_000002.11:g.116510817G>T
DPP10 transcript variant 1 NM_020868.6:c.1018= NM_020868.6:c.1018G>A NM_020868.6:c.1018G>C NM_020868.6:c.1018G>T
DPP10 transcript variant 1 NM_020868.5:c.1018= NM_020868.5:c.1018G>A NM_020868.5:c.1018G>C NM_020868.5:c.1018G>T
DPP10 transcript variant 1 NM_020868.4:c.1018= NM_020868.4:c.1018G>A NM_020868.4:c.1018G>C NM_020868.4:c.1018G>T
DPP10 transcript variant 1 NM_020868.3:c.1018= NM_020868.3:c.1018G>A NM_020868.3:c.1018G>C NM_020868.3:c.1018G>T
DPP10 transcript variant 2 NM_001004360.5:c.997= NM_001004360.5:c.997G>A NM_001004360.5:c.997G>C NM_001004360.5:c.997G>T
DPP10 transcript variant 2 NM_001004360.4:c.997= NM_001004360.4:c.997G>A NM_001004360.4:c.997G>C NM_001004360.4:c.997G>T
DPP10 transcript variant 2 NM_001004360.3:c.997= NM_001004360.3:c.997G>A NM_001004360.3:c.997G>C NM_001004360.3:c.997G>T
DPP10 transcript variant 6 NM_001321905.3:c.1069= NM_001321905.3:c.1069G>A NM_001321905.3:c.1069G>C NM_001321905.3:c.1069G>T
DPP10 transcript variant 6 NM_001321905.2:c.1069= NM_001321905.2:c.1069G>A NM_001321905.2:c.1069G>C NM_001321905.2:c.1069G>T
DPP10 transcript variant 6 NM_001321905.1:c.1069= NM_001321905.1:c.1069G>A NM_001321905.1:c.1069G>C NM_001321905.1:c.1069G>T
DPP10 transcript variant 5 NM_001178036.3:c.868= NM_001178036.3:c.868G>A NM_001178036.3:c.868G>C NM_001178036.3:c.868G>T
DPP10 transcript variant 5 NM_001178036.2:c.868= NM_001178036.2:c.868G>A NM_001178036.2:c.868G>C NM_001178036.2:c.868G>T
DPP10 transcript variant 5 NM_001178036.1:c.868= NM_001178036.1:c.868G>A NM_001178036.1:c.868G>C NM_001178036.1:c.868G>T
DPP10 transcript variant 12 NM_001321911.3:c.868= NM_001321911.3:c.868G>A NM_001321911.3:c.868G>C NM_001321911.3:c.868G>T
DPP10 transcript variant 12 NM_001321911.2:c.868= NM_001321911.2:c.868G>A NM_001321911.2:c.868G>C NM_001321911.2:c.868G>T
DPP10 transcript variant 12 NM_001321911.1:c.868= NM_001321911.1:c.868G>A NM_001321911.1:c.868G>C NM_001321911.1:c.868G>T
DPP10 transcript variant 13 NM_001321912.3:c.868= NM_001321912.3:c.868G>A NM_001321912.3:c.868G>C NM_001321912.3:c.868G>T
DPP10 transcript variant 13 NM_001321912.2:c.868= NM_001321912.2:c.868G>A NM_001321912.2:c.868G>C NM_001321912.2:c.868G>T
DPP10 transcript variant 13 NM_001321912.1:c.868= NM_001321912.1:c.868G>A NM_001321912.1:c.868G>C NM_001321912.1:c.868G>T
DPP10 transcript variant 9 NM_001321908.3:c.928= NM_001321908.3:c.928G>A NM_001321908.3:c.928G>C NM_001321908.3:c.928G>T
DPP10 transcript variant 9 NM_001321908.2:c.928= NM_001321908.2:c.928G>A NM_001321908.2:c.928G>C NM_001321908.2:c.928G>T
DPP10 transcript variant 9 NM_001321908.1:c.928= NM_001321908.1:c.928G>A NM_001321908.1:c.928G>C NM_001321908.1:c.928G>T
DPP10 transcript variant 11 NM_001321910.3:c.868= NM_001321910.3:c.868G>A NM_001321910.3:c.868G>C NM_001321910.3:c.868G>T
DPP10 transcript variant 11 NM_001321910.2:c.868= NM_001321910.2:c.868G>A NM_001321910.2:c.868G>C NM_001321910.2:c.868G>T
DPP10 transcript variant 11 NM_001321910.1:c.868= NM_001321910.1:c.868G>A NM_001321910.1:c.868G>C NM_001321910.1:c.868G>T
DPP10 transcript variant 4 NM_001178037.3:c.1006= NM_001178037.3:c.1006G>A NM_001178037.3:c.1006G>C NM_001178037.3:c.1006G>T
DPP10 transcript variant 4 NM_001178037.2:c.1006= NM_001178037.2:c.1006G>A NM_001178037.2:c.1006G>C NM_001178037.2:c.1006G>T
DPP10 transcript variant 4 NM_001178037.1:c.1006= NM_001178037.1:c.1006G>A NM_001178037.1:c.1006G>C NM_001178037.1:c.1006G>T
DPP10 transcript variant 8 NM_001321907.3:c.1018= NM_001321907.3:c.1018G>A NM_001321907.3:c.1018G>C NM_001321907.3:c.1018G>T
DPP10 transcript variant 8 NM_001321907.2:c.1018= NM_001321907.2:c.1018G>A NM_001321907.2:c.1018G>C NM_001321907.2:c.1018G>T
DPP10 transcript variant 8 NM_001321907.1:c.1018= NM_001321907.1:c.1018G>A NM_001321907.1:c.1018G>C NM_001321907.1:c.1018G>T
DPP10 transcript variant 14 NM_001321913.3:c.256= NM_001321913.3:c.256G>A NM_001321913.3:c.256G>C NM_001321913.3:c.256G>T
DPP10 transcript variant 14 NM_001321913.2:c.256= NM_001321913.2:c.256G>A NM_001321913.2:c.256G>C NM_001321913.2:c.256G>T
DPP10 transcript variant 14 NM_001321913.1:c.256= NM_001321913.1:c.256G>A NM_001321913.1:c.256G>C NM_001321913.1:c.256G>T
DPP10 transcript variant 10 NM_001321909.3:c.901= NM_001321909.3:c.901G>A NM_001321909.3:c.901G>C NM_001321909.3:c.901G>T
DPP10 transcript variant 10 NM_001321909.2:c.901= NM_001321909.2:c.901G>A NM_001321909.2:c.901G>C NM_001321909.2:c.901G>T
DPP10 transcript variant 10 NM_001321909.1:c.901= NM_001321909.1:c.901G>A NM_001321909.1:c.901G>C NM_001321909.1:c.901G>T
DPP10 transcript variant 7 NM_001321906.2:c.997= NM_001321906.2:c.997G>A NM_001321906.2:c.997G>C NM_001321906.2:c.997G>T
DPP10 transcript variant 7 NM_001321906.1:c.997= NM_001321906.1:c.997G>A NM_001321906.1:c.997G>C NM_001321906.1:c.997G>T
DPP10 transcript variant 15 NM_001321914.2:c.256= NM_001321914.2:c.256G>A NM_001321914.2:c.256G>C NM_001321914.2:c.256G>T
DPP10 transcript variant 15 NM_001321914.1:c.256= NM_001321914.1:c.256G>A NM_001321914.1:c.256G>C NM_001321914.1:c.256G>T
DPP10 transcript variant X2 XM_017004566.1:c.895= XM_017004566.1:c.895G>A XM_017004566.1:c.895G>C XM_017004566.1:c.895G>T
DPP10 transcript variant 3 NM_001178034.1:c.1030= NM_001178034.1:c.1030G>A NM_001178034.1:c.1030G>C NM_001178034.1:c.1030G>T
DPP10 transcript variant X1 XM_024453023.1:c.997= XM_024453023.1:c.997G>A XM_024453023.1:c.997G>C XM_024453023.1:c.997G>T
inactive dipeptidyl peptidase 10 isoform long NP_065919.3:p.Ala340= NP_065919.3:p.Ala340Thr NP_065919.3:p.Ala340Pro NP_065919.3:p.Ala340Ser
inactive dipeptidyl peptidase 10 isoform short NP_001004360.3:p.Ala333= NP_001004360.3:p.Ala333Thr NP_001004360.3:p.Ala333Pro NP_001004360.3:p.Ala333Ser
inactive dipeptidyl peptidase 10 isoform d NP_001308834.2:p.Ala357= NP_001308834.2:p.Ala357Thr NP_001308834.2:p.Ala357Pro NP_001308834.2:p.Ala357Ser
inactive dipeptidyl peptidase 10 isoform a NP_001171507.2:p.Ala290= NP_001171507.2:p.Ala290Thr NP_001171507.2:p.Ala290Pro NP_001171507.2:p.Ala290Ser
inactive dipeptidyl peptidase 10 isoform a NP_001308840.2:p.Ala290= NP_001308840.2:p.Ala290Thr NP_001308840.2:p.Ala290Pro NP_001308840.2:p.Ala290Ser
inactive dipeptidyl peptidase 10 isoform h NP_001308841.2:p.Ala290= NP_001308841.2:p.Ala290Thr NP_001308841.2:p.Ala290Pro NP_001308841.2:p.Ala290Ser
inactive dipeptidyl peptidase 10 isoform f NP_001308837.2:p.Ala310= NP_001308837.2:p.Ala310Thr NP_001308837.2:p.Ala310Pro NP_001308837.2:p.Ala310Ser
inactive dipeptidyl peptidase 10 isoform a NP_001308839.2:p.Ala290= NP_001308839.2:p.Ala290Thr NP_001308839.2:p.Ala290Pro NP_001308839.2:p.Ala290Ser
inactive dipeptidyl peptidase 10 isoform b NP_001171508.2:p.Ala336= NP_001171508.2:p.Ala336Thr NP_001171508.2:p.Ala336Pro NP_001171508.2:p.Ala336Ser
inactive dipeptidyl peptidase 10 isoform e NP_001308836.2:p.Ala340= NP_001308836.2:p.Ala340Thr NP_001308836.2:p.Ala340Pro NP_001308836.2:p.Ala340Ser
inactive dipeptidyl peptidase 10 isoform i NP_001308842.2:p.Ala86= NP_001308842.2:p.Ala86Thr NP_001308842.2:p.Ala86Pro NP_001308842.2:p.Ala86Ser
inactive dipeptidyl peptidase 10 isoform g NP_001308838.2:p.Ala301= NP_001308838.2:p.Ala301Thr NP_001308838.2:p.Ala301Pro NP_001308838.2:p.Ala301Ser
inactive dipeptidyl peptidase 10 isoform short NP_001308835.2:p.Ala333= NP_001308835.2:p.Ala333Thr NP_001308835.2:p.Ala333Pro NP_001308835.2:p.Ala333Ser
inactive dipeptidyl peptidase 10 isoform i NP_001308843.2:p.Ala86= NP_001308843.2:p.Ala86Thr NP_001308843.2:p.Ala86Pro NP_001308843.2:p.Ala86Ser
inactive dipeptidyl peptidase 10 isoform X2 XP_016860055.1:p.Ala299= XP_016860055.1:p.Ala299Thr XP_016860055.1:p.Ala299Pro XP_016860055.1:p.Ala299Ser
inactive dipeptidyl peptidase 10 isoform c NP_001171505.1:p.Ala344= NP_001171505.1:p.Ala344Thr NP_001171505.1:p.Ala344Pro NP_001171505.1:p.Ala344Ser
inactive dipeptidyl peptidase 10 isoform X1 XP_024308791.1:p.Ala333= XP_024308791.1:p.Ala333Thr XP_024308791.1:p.Ala333Pro XP_024308791.1:p.Ala333Ser
inactive dipeptidyl peptidase 10 isoform short NP_001004360.2:p.Ala333= NP_001004360.2:p.Ala333Thr NP_001004360.2:p.Ala333Pro NP_001004360.2:p.Ala333Ser
inactive dipeptidyl peptidase 10 isoform a NP_001171507.1:p.Ala290= NP_001171507.1:p.Ala290Thr NP_001171507.1:p.Ala290Pro NP_001171507.1:p.Ala290Ser
inactive dipeptidyl peptidase 10 isoform b NP_001171508.1:p.Ala336= NP_001171508.1:p.Ala336Thr NP_001171508.1:p.Ala336Pro NP_001171508.1:p.Ala336Ser
inactive dipeptidyl peptidase 10 isoform long NP_065919.2:p.Ala340= NP_065919.2:p.Ala340Thr NP_065919.2:p.Ala340Pro NP_065919.2:p.Ala340Ser
Help

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#.

111 SubSNP, 25 Frequency submissions
No Submitter Submission ID Date (Build)
1 TSC-CSHL ss2964339 Apr 12, 2001 (94)
2 CSHL-HAPMAP ss16851618 Feb 27, 2004 (120)
3 CSHL-HAPMAP ss19443629 Feb 27, 2004 (120)
4 SSAHASNP ss21589187 Apr 05, 2004 (121)
5 ABI ss44342686 Mar 13, 2006 (126)
6 APPLERA_GI ss48407202 Mar 13, 2006 (126)
7 PERLEGEN ss68825143 May 17, 2007 (127)
8 AFFY ss74809978 Aug 16, 2007 (128)
9 HGSV ss77180966 Dec 06, 2007 (129)
10 KRIBB_YJKIM ss80761752 Dec 15, 2007 (130)
11 HGSV ss81901520 Dec 15, 2007 (130)
12 BCMHGSC_JDW ss91306258 Mar 24, 2008 (129)
13 HUMANGENOME_JCVI ss97068490 Feb 06, 2009 (130)
14 BGI ss103563237 Dec 01, 2009 (131)
15 1000GENOMES ss109802020 Jan 24, 2009 (130)
16 ENSEMBL ss136186461 Dec 01, 2009 (131)
17 ENSEMBL ss138510696 Dec 01, 2009 (131)
18 GMI ss157533624 Dec 01, 2009 (131)
19 SEATTLESEQ ss159702666 Dec 01, 2009 (131)
20 ILLUMINA ss160494869 Dec 01, 2009 (131)
21 BUSHMAN ss200913231 Jul 04, 2010 (132)
22 BCM-HGSC-SUB ss205698406 Jul 04, 2010 (132)
23 1000GENOMES ss219449004 Jul 14, 2010 (132)
24 1000GENOMES ss231318221 Jul 14, 2010 (132)
25 1000GENOMES ss238837553 Jul 15, 2010 (132)
26 BL ss253391677 May 09, 2011 (134)
27 RSG_JCVI ss262866771 May 09, 2011 (134)
28 GMI ss276631976 May 04, 2012 (137)
29 GMI ss284416755 Apr 25, 2013 (138)
30 PJP ss292346243 May 09, 2011 (134)
31 NHLBI-ESP ss342075780 May 09, 2011 (134)
32 ILLUMINA ss480400389 May 04, 2012 (137)
33 ILLUMINA ss480413573 May 04, 2012 (137)
34 ILLUMINA ss481194102 Sep 08, 2015 (146)
35 ILLUMINA ss484997805 May 04, 2012 (137)
36 1000GENOMES ss489829896 May 04, 2012 (137)
37 EXOME_CHIP ss491323514 May 04, 2012 (137)
38 CLINSEQ_SNP ss491790170 May 04, 2012 (137)
39 ILLUMINA ss537030280 Sep 08, 2015 (146)
40 SSMP ss649427128 Apr 25, 2013 (138)
41 ILLUMINA ss778342343 Sep 08, 2015 (146)
42 ILLUMINA ss782945203 Sep 08, 2015 (146)
43 ILLUMINA ss783907692 Sep 08, 2015 (146)
44 ILLUMINA ss832200974 Sep 08, 2015 (146)
45 ILLUMINA ss833796954 Sep 08, 2015 (146)
46 JMKIDD_LAB ss974443479 Aug 21, 2014 (142)
47 EVA-GONL ss977243774 Aug 21, 2014 (142)
48 JMKIDD_LAB ss1067440361 Aug 21, 2014 (142)
49 JMKIDD_LAB ss1069408920 Aug 21, 2014 (142)
50 1000GENOMES ss1298875199 Aug 21, 2014 (142)
51 DDI ss1428700457 Apr 01, 2015 (144)
52 EVA_GENOME_DK ss1579040663 Apr 01, 2015 (144)
53 EVA_FINRISK ss1584020540 Apr 01, 2015 (144)
54 EVA_DECODE ss1586668310 Apr 01, 2015 (144)
55 EVA_UK10K_ALSPAC ss1604337833 Apr 01, 2015 (144)
56 EVA_UK10K_TWINSUK ss1647331866 Apr 01, 2015 (144)
57 EVA_EXAC ss1686481365 Apr 01, 2015 (144)
58 EVA_MGP ss1710977290 Apr 01, 2015 (144)
59 HAMMER_LAB ss1797332126 Sep 08, 2015 (146)
60 WEILL_CORNELL_DGM ss1920492388 Feb 12, 2016 (147)
61 GENOMED ss1968861023 Jul 19, 2016 (147)
62 JJLAB ss2020774535 Sep 14, 2016 (149)
63 USC_VALOUEV ss2148831334 Dec 20, 2016 (150)
64 HUMAN_LONGEVITY ss2233443419 Dec 20, 2016 (150)
65 TOPMED ss2399695027 Dec 20, 2016 (150)
66 SYSTEMSBIOZJU ss2624893224 Nov 08, 2017 (151)
67 GRF ss2703443087 Nov 08, 2017 (151)
68 GNOMAD ss2732934860 Nov 08, 2017 (151)
69 GNOMAD ss2746763331 Nov 08, 2017 (151)
70 GNOMAD ss2778371392 Nov 08, 2017 (151)
71 AFFY ss2985182883 Nov 08, 2017 (151)
72 SWEGEN ss2990232258 Nov 08, 2017 (151)
73 EVA_SAMSUNG_MC ss3023058517 Nov 08, 2017 (151)
74 BIOINF_KMB_FNS_UNIBA ss3024149269 Nov 08, 2017 (151)
75 TOPMED ss3320053535 Nov 08, 2017 (151)
76 TOPMED ss3320053536 Nov 08, 2017 (151)
77 CSHL ss3344421794 Nov 08, 2017 (151)
78 ILLUMINA ss3628145037 Oct 11, 2018 (152)
79 ILLUMINA ss3631625050 Oct 11, 2018 (152)
80 ILLUMINA ss3633213138 Oct 11, 2018 (152)
81 ILLUMINA ss3633925394 Oct 11, 2018 (152)
82 ILLUMINA ss3636471736 Oct 11, 2018 (152)
83 OMUKHERJEE_ADBS ss3646269937 Oct 11, 2018 (152)
84 URBANLAB ss3647119162 Oct 11, 2018 (152)
85 ILLUMINA ss3653949442 Oct 11, 2018 (152)
86 EGCUT_WGS ss3658104123 Jul 13, 2019 (153)
87 EVA_DECODE ss3704679203 Jul 13, 2019 (153)
88 ACPOP ss3728772085 Jul 13, 2019 (153)
89 EVA ss3757245601 Jul 13, 2019 (153)
90 PACBIO ss3783965449 Jul 13, 2019 (153)
91 PACBIO ss3789533696 Jul 13, 2019 (153)
92 PACBIO ss3794406486 Jul 13, 2019 (153)
93 KHV_HUMAN_GENOMES ss3801612278 Jul 13, 2019 (153)
94 EVA ss3823803228 Apr 25, 2020 (154)
95 EVA ss3825519840 Apr 25, 2020 (154)
96 EVA ss3825536560 Apr 25, 2020 (154)
97 EVA ss3825607730 Apr 25, 2020 (154)
98 EVA ss3827166207 Apr 25, 2020 (154)
99 EVA ss3836997763 Apr 25, 2020 (154)
100 EVA ss3842416268 Apr 25, 2020 (154)
101 SGDP_PRJ ss3853164612 Apr 25, 2020 (154)
102 KRGDB ss3898720531 Apr 25, 2020 (154)
103 FSA-LAB ss3984186645 Apr 26, 2021 (155)
104 FSA-LAB ss3984186646 Apr 26, 2021 (155)
105 EVA ss3984488202 Apr 26, 2021 (155)
106 EVA ss3986019070 Apr 26, 2021 (155)
107 EVA ss3986194523 Apr 26, 2021 (155)
108 TOPMED ss4520121234 Apr 26, 2021 (155)
109 TOMMO_GENOMICS ss5153352185 Apr 26, 2021 (155)
110 EVA ss5236973444 Apr 26, 2021 (155)
111 EVA ss5237171233 Apr 26, 2021 (155)
112 1000Genomes NC_000002.11 - 116510817 Oct 11, 2018 (152)
113 The Avon Longitudinal Study of Parents and Children NC_000002.11 - 116510817 Oct 11, 2018 (152)
114 Genetic variation in the Estonian population NC_000002.11 - 116510817 Oct 11, 2018 (152)
115 ExAC NC_000002.11 - 116510817 Oct 11, 2018 (152)
116 FINRISK NC_000002.11 - 116510817 Apr 25, 2020 (154)
117 The Danish reference pan genome NC_000002.11 - 116510817 Apr 25, 2020 (154)
118 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 70549203 (NC_000002.12:115753240:G:A 1/140016)
Row 70549204 (NC_000002.12:115753240:G:C 71442/139950)

- Apr 26, 2021 (155)
119 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 70549203 (NC_000002.12:115753240:G:A 1/140016)
Row 70549204 (NC_000002.12:115753240:G:C 71442/139950)

- Apr 26, 2021 (155)
120 gnomAD - Exomes

Submission ignored due to conflicting rows:
Row 1991276 (NC_000002.11:116510816:G:G 93741/250074, NC_000002.11:116510816:G:C 156333/250074)
Row 1991277 (NC_000002.11:116510816:G:G 250073/250074, NC_000002.11:116510816:G:T 1/250074)

- Jul 13, 2019 (153)
121 gnomAD - Exomes

Submission ignored due to conflicting rows:
Row 1991276 (NC_000002.11:116510816:G:G 93741/250074, NC_000002.11:116510816:G:C 156333/250074)
Row 1991277 (NC_000002.11:116510816:G:G 250073/250074, NC_000002.11:116510816:G:T 1/250074)

- Jul 13, 2019 (153)
122 GO Exome Sequencing Project NC_000002.11 - 116510817 Oct 11, 2018 (152)
123 Genome of the Netherlands Release 5 NC_000002.11 - 116510817 Apr 25, 2020 (154)
124 HapMap NC_000002.12 - 115753241 Apr 25, 2020 (154)
125 KOREAN population from KRGDB NC_000002.11 - 116510817 Apr 25, 2020 (154)
126 Medical Genome Project healthy controls from Spanish population NC_000002.11 - 116510817 Apr 25, 2020 (154)
127 Northern Sweden NC_000002.11 - 116510817 Jul 13, 2019 (153)
128 CNV burdens in cranial meningiomas NC_000002.11 - 116510817 Apr 26, 2021 (155)
129 Qatari NC_000002.11 - 116510817 Apr 25, 2020 (154)
130 SGDP_PRJ NC_000002.11 - 116510817 Apr 25, 2020 (154)
131 Siberian NC_000002.11 - 116510817 Apr 25, 2020 (154)
132 8.3KJPN NC_000002.11 - 116510817 Apr 26, 2021 (155)
133 TopMed NC_000002.12 - 115753241 Apr 26, 2021 (155)
134 UK 10K study - Twins NC_000002.11 - 116510817 Oct 11, 2018 (152)
135 A Vietnamese Genetic Variation Database NC_000002.11 - 116510817 Jul 13, 2019 (153)
136 ALFA NC_000002.12 - 115753241 Apr 26, 2021 (155)
Help

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)
rs52799400 Sep 21, 2007 (128)
rs60675889 May 26, 2008 (130)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
ss2746763331, ss2778371392 NC_000002.11:116510816:G:A NC_000002.12:115753240:G:A (self)
1684265018, ss3320053535 NC_000002.12:115753240:G:A NC_000002.12:115753240:G:A (self)
ss77180966, ss81901520 NC_000002.9:116227046:G:C NC_000002.12:115753240:G:C (self)
ss91306258, ss109802020, ss200913231, ss205698406, ss253391677, ss276631976, ss284416755, ss292346243, ss480400389, ss491790170, ss1586668310 NC_000002.10:116227286:G:C NC_000002.12:115753240:G:C (self)
9875827, 5448260, 3842371, 6365897, 17001, 5206872, 261663, 2394311, 5897925, 93907, 2056950, 37536, 2534318, 5181592, 1347688, 11321492, 5448260, 1180741, ss219449004, ss231318221, ss238837553, ss342075780, ss480413573, ss481194102, ss484997805, ss489829896, ss491323514, ss537030280, ss649427128, ss778342343, ss782945203, ss783907692, ss832200974, ss833796954, ss974443479, ss977243774, ss1067440361, ss1069408920, ss1298875199, ss1428700457, ss1579040663, ss1584020540, ss1604337833, ss1647331866, ss1686481365, ss1710977290, ss1797332126, ss1920492388, ss1968861023, ss2020774535, ss2148831334, ss2399695027, ss2624893224, ss2703443087, ss2732934860, ss2746763331, ss2778371392, ss2985182883, ss2990232258, ss3023058517, ss3344421794, ss3628145037, ss3631625050, ss3633213138, ss3633925394, ss3636471736, ss3646269937, ss3653949442, ss3658104123, ss3728772085, ss3757245601, ss3783965449, ss3789533696, ss3794406486, ss3823803228, ss3825519840, ss3825536560, ss3825607730, ss3827166207, ss3836997763, ss3853164612, ss3898720531, ss3984186645, ss3984186646, ss3984488202, ss3986019070, ss3986194523, ss5153352185 NC_000002.11:116510816:G:C NC_000002.12:115753240:G:C (self)
1872660, 202102954, 323944113, 1684265018, ss2233443419, ss3024149269, ss3320053536, ss3647119162, ss3704679203, ss3801612278, ss3842416268, ss4520121234, ss5236973444, ss5237171233 NC_000002.12:115753240:G:C NC_000002.12:115753240:G:C (self)
ss16851618, ss19443629, ss21589187 NT_022135.13:5218558:G:C NC_000002.12:115753240:G:C (self)
ss2964339, ss44342686, ss48407202, ss68825143, ss74809978, ss80761752, ss97068490, ss103563237, ss136186461, ss138510696, ss157533624, ss159702666, ss160494869, ss262866771 NT_022135.16:6259479:G:C NC_000002.12:115753240:G:C (self)
5897925, ss2732934860, ss3898720531 NC_000002.11:116510816:G:T NC_000002.12:115753240:G:T (self)
Help

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

1 citation for rs2053724
PMID Title Author Year Journal
33384710 The Co-existence of ADHD With Autism in Saudi Children: An Analysis Using Next-Generation DNA Sequencing. Bogari NM et al. 2020 Frontiers in genetics
Help

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.

Software version is: 2.0.1.post596+ae089ad