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dbSNP Short Genetic Variations

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.


Current Build 153

Released July 9, 2019

Homo sapiens
chr19:3565255 (GRCh38.p12) 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.

G>A / G>C
Variation Type
SNV Single Nucleotide Variation
A=0.27426 (34438/125568, TOPMED)
A=0.2577 (8026/31150, GnomAD)
A=0.357 (1790/5008, 1000G) (+ 4 more)
A=0.080 (357/4478, Estonian)
A=0.067 (258/3854, ALSPAC)
A=0.060 (222/3708, TWINSUK)
A=0.05 (30/600, NorthernSweden)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
0 citations
Genomic View
See rs on genome

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.p12 chr 19 NC_000019.10:g.3565255G>A
GRCh38.p12 chr 19 NC_000019.10:g.3565255G>C
GRCh37.p13 chr 19 NC_000019.9:g.3565253G>A
GRCh37.p13 chr 19 NC_000019.9:g.3565253G>C

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

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").

Study Population Group Sample Size Ref Allele Alt Allele
TopMed Global Study-wide 125568 G=0.72574 A=0.27426
gnomAD - Genomes Global Study-wide 31150 G=0.7423 A=0.2577
gnomAD - Genomes European Sub 18738 G=0.9215 A=0.0785
gnomAD - Genomes African Sub 8646 G=0.294 A=0.706
gnomAD - Genomes East Asian Sub 1550 G=0.945 A=0.055
gnomAD - Genomes Other Sub 1078 G=0.846 A=0.154
gnomAD - Genomes American Sub 848 G=0.82 A=0.18
gnomAD - Genomes Ashkenazi Jewish Sub 290 G=0.84 A=0.16
1000Genomes Global Study-wide 5008 G=0.643 A=0.357
1000Genomes African Sub 1322 G=0.164 A=0.836
1000Genomes East Asian Sub 1008 G=0.952 A=0.048
1000Genomes Europe Sub 1006 G=0.938 A=0.062
1000Genomes South Asian Sub 978 G=0.54 A=0.46
1000Genomes American Sub 694 G=0.82 A=0.18
Genetic variation in the Estonian population Estonian Study-wide 4478 G=0.920 A=0.080
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 G=0.933 A=0.067
UK 10K study - Twins TWIN COHORT Study-wide 3708 G=0.940 A=0.060
Northern Sweden ACPOP Study-wide 600 G=0.95 A=0.05

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 Note
GRCh38.p12 chr 19 NC_000019.10:g.35...






GRCh37.p13 chr 19 NC_000019.9:g.356...







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, 7 Frequency submissions
No Submitter Submission ID Date (Build)
1 BCM_SSAHASNP ss10944784 Jul 11, 2003 (116)
2 WI_SSAHASNP ss12474114 Jul 11, 2003 (116)
3 CSHL-HAPMAP ss17612807 Feb 27, 2004 (120)
4 ABI ss41050516 Mar 14, 2006 (126)
5 1000GENOMES ss340281232 May 09, 2011 (134)
6 TISHKOFF ss565818312 Apr 25, 2013 (138)
7 SSMP ss661670817 Apr 25, 2013 (138)
8 EVA-GONL ss994028487 Aug 21, 2014 (142)
9 JMKIDD_LAB ss1081721026 Aug 21, 2014 (142)
10 1000GENOMES ss1362127996 Aug 21, 2014 (142)
11 DDI ss1428317174 Apr 01, 2015 (144)
12 EVA_GENOME_DK ss1578532148 Apr 01, 2015 (144)
13 EVA_UK10K_ALSPAC ss1637459311 Apr 01, 2015 (144)
14 EVA_UK10K_TWINSUK ss1680453344 Apr 01, 2015 (144)
15 EVA_DECODE ss1698090781 Apr 01, 2015 (144)
16 HAMMER_LAB ss1809180377 Sep 08, 2015 (146)
17 WEILL_CORNELL_DGM ss1937507037 Feb 12, 2016 (147)
18 GENOMED ss1968595094 Jul 19, 2016 (147)
19 JJLAB ss2029528542 Sep 14, 2016 (149)
20 USC_VALOUEV ss2158042967 Dec 20, 2016 (150)
21 HUMAN_LONGEVITY ss2223836721 Dec 20, 2016 (150)
22 TOPMED ss2389264031 Dec 20, 2016 (150)
23 GRF ss2702646255 Nov 08, 2017 (151)
24 GNOMAD ss2959796582 Nov 08, 2017 (151)
25 SWEGEN ss3016991473 Nov 08, 2017 (151)
26 TOPMED ss3286386084 Nov 08, 2017 (151)
27 TOPMED ss3286386085 Nov 08, 2017 (151)
28 BIOINF_KMB_FNS_UNIBA ss3645504627 Oct 12, 2018 (152)
29 EGCUT_WGS ss3683837775 Jul 13, 2019 (153)
30 EVA_DECODE ss3702222122 Jul 13, 2019 (153)
31 ACPOP ss3742802178 Jul 13, 2019 (153)
32 EVA ss3755742018 Jul 13, 2019 (153)
33 PACBIO ss3788450843 Jul 13, 2019 (153)
34 PACBIO ss3793373681 Jul 13, 2019 (153)
35 PACBIO ss3798260247 Jul 13, 2019 (153)
36 KHV_HUMAN_GENOMES ss3820996267 Jul 13, 2019 (153)
37 1000Genomes NC_000019.9 - 3565253 Oct 12, 2018 (152)
38 The Avon Longitudinal Study of Parents and Children NC_000019.9 - 3565253 Oct 12, 2018 (152)
39 Genetic variation in the Estonian population NC_000019.9 - 3565253 Oct 12, 2018 (152)
40 gnomAD - Genomes NC_000019.9 - 3565253 Jul 13, 2019 (153)
41 Northern Sweden NC_000019.9 - 3565253 Jul 13, 2019 (153)
42 TopMed NC_000019.10 - 3565255 Oct 12, 2018 (152)
43 UK 10K study - Twins NC_000019.9 - 3565253 Oct 12, 2018 (152)

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).

Added to this RefSNP Cluster:
Submission ids Observation SPDI Canonical SPDI Source RSIDs
ss1698090781 NC_000019.8:3516252:G:A NC_000019.10:3565254:G:A (self)
75496550, 41841755, 29576023, 206057003, 16087043, 41841755, ss340281232, ss565818312, ss661670817, ss994028487, ss1081721026, ss1362127996, ss1428317174, ss1578532148, ss1637459311, ss1680453344, ss1809180377, ss1937507037, ss1968595094, ss2029528542, ss2158042967, ss2389264031, ss2702646255, ss2959796582, ss3016991473, ss3683837775, ss3742802178, ss3755742018, ss3788450843, ss3793373681, ss3798260247 NC_000019.9:3565252:G:A NC_000019.10:3565254:G:A (self)
175741185, ss2223836721, ss3286386084, ss3645504627, ss3702222122, ss3820996267 NC_000019.10:3565254:G:A NC_000019.10:3565254:G:A (self)
ss10944784, ss12474114 NT_011255.13:3505252:G:A NC_000019.10:3565254:G:A (self)
ss17612807, ss41050516 NT_011255.14:3505252:G:A NC_000019.10:3565254:G:A (self)
ss3286386085 NC_000019.10:3565254:G:C NC_000019.10:3565254:G:C (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 rs6510760

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.post104+4a6ee9c