Name: rs6915982
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.

rs6915982

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr6:3419197 (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: A>C / A>G / A>T
Variation Type: SNV Single Nucleotide Variation
Frequency: A=0.057769 (15291/264690, TOPMED)
A=0.050884 (7136/140240, GnomAD)
A=0.04201 (1301/30966, ALFA) (+ 18 more)
A=0.04947 (1398/28258, 14KJPN)
A=0.05042 (845/16760, 8.3KJPN)
A=0.0631 (404/6404, 1000G_30x)
A=0.0615 (308/5008, 1000G)
A=0.0362 (162/4480, Estonian)
A=0.0389 (150/3854, ALSPAC)
A=0.0386 (143/3708, TWINSUK)
A=0.0369 (108/2930, KOREAN)
A=0.0273 (50/1832, Korea1K)
A=0.0434 (49/1130, Daghestan)
A=0.045 (45/998, GoNL)
A=0.047 (32/680, HapMap)
A=0.063 (38/600, NorthernSweden)
A=0.054 (30/556, SGDP_PRJ)
A=0.028 (6/216, Qatari)
A=0.032 (7/216, Vietnamese)
A=0.02 (1/56, Siberian)
A=0.03 (1/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: SLC22A23 : Intron Variant
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	30966	A=0.04201	G=0.95799
European	Sub	24814	A=0.03695	G=0.96305
African	Sub	3172	A=0.0523	G=0.9477
African Others	Sub	124	A=0.048	G=0.952
African American	Sub	3048	A=0.0525	G=0.9475
Asian	Sub	130	A=0.008	G=0.992
East Asian	Sub	102	A=0.010	G=0.990
Other Asian	Sub	28	A=0.00	G=1.00
Latin American 1	Sub	168	A=0.054	G=0.946
Latin American 2	Sub	700	A=0.164	G=0.836
South Asian	Sub	116	A=0.069	G=0.931
Other	Sub	1866	A=0.0456	G=0.9544

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	A=0.057769	G=0.942231
gnomAD - Genomes	Global	Study-wide	140240	A=0.050884	G=0.949116
gnomAD - Genomes	European	Sub	75964	A=0.03764	G=0.96236
gnomAD - Genomes	African	Sub	42008	A=0.05439	G=0.94561
gnomAD - Genomes	American	Sub	13660	A=0.12848	G=0.87152
gnomAD - Genomes	Ashkenazi Jewish	Sub	3324	A=0.0111	G=0.9889
gnomAD - Genomes	East Asian	Sub	3132	A=0.0249	G=0.9751
gnomAD - Genomes	Other	Sub	2152	A=0.0567	G=0.9433
Allele Frequency Aggregator	Total	Global	30966	A=0.04201	G=0.95799
Allele Frequency Aggregator	European	Sub	24814	A=0.03695	G=0.96305
Allele Frequency Aggregator	African	Sub	3172	A=0.0523	G=0.9477
Allele Frequency Aggregator	Other	Sub	1866	A=0.0456	G=0.9544
Allele Frequency Aggregator	Latin American 2	Sub	700	A=0.164	G=0.836
Allele Frequency Aggregator	Latin American 1	Sub	168	A=0.054	G=0.946
Allele Frequency Aggregator	Asian	Sub	130	A=0.008	G=0.992
Allele Frequency Aggregator	South Asian	Sub	116	A=0.069	G=0.931
14KJPN	JAPANESE	Study-wide	28258	A=0.04947	G=0.95053
8.3KJPN	JAPANESE	Study-wide	16760	A=0.05042	G=0.94958
1000Genomes_30x	Global	Study-wide	6404	A=0.0631	G=0.9369
1000Genomes_30x	African	Sub	1786	A=0.0543	G=0.9457
1000Genomes_30x	Europe	Sub	1266	A=0.0316	G=0.9684
1000Genomes_30x	South Asian	Sub	1202	A=0.0416	G=0.9584
1000Genomes_30x	East Asian	Sub	1170	A=0.0342	G=0.9658
1000Genomes_30x	American	Sub	980	A=0.181	G=0.819
1000Genomes	Global	Study-wide	5008	A=0.0615	G=0.9385
1000Genomes	African	Sub	1322	A=0.0537	G=0.9463
1000Genomes	East Asian	Sub	1008	A=0.0327	G=0.9673
1000Genomes	Europe	Sub	1006	A=0.0338	G=0.9662
1000Genomes	South Asian	Sub	978	A=0.047	G=0.953
1000Genomes	American	Sub	694	A=0.179	G=0.821
Genetic variation in the Estonian population	Estonian	Study-wide	4480	A=0.0362	G=0.9638
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	A=0.0389	G=0.9611
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	A=0.0386	G=0.9614
KOREAN population from KRGDB	KOREAN	Study-wide	2930	A=0.0369	C=0.0000, G=0.9631, T=0.0000
Korean Genome Project	KOREAN	Study-wide	1832	A=0.0273	G=0.9727
Genome-wide autozygosity in Daghestan	Global	Study-wide	1130	A=0.0434	G=0.9566
Genome-wide autozygosity in Daghestan	Daghestan	Sub	626	A=0.043	G=0.957
Genome-wide autozygosity in Daghestan	Near_East	Sub	144	A=0.049	G=0.951
Genome-wide autozygosity in Daghestan	Central Asia	Sub	122	A=0.041	G=0.959
Genome-wide autozygosity in Daghestan	Europe	Sub	106	A=0.028	G=0.972
Genome-wide autozygosity in Daghestan	South Asian	Sub	96	A=0.06	G=0.94
Genome-wide autozygosity in Daghestan	Caucasus	Sub	36	A=0.03	G=0.97
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	A=0.045	G=0.955
HapMap	Global	Study-wide	680	A=0.047	G=0.953
HapMap	Asian	Sub	242	A=0.050	G=0.950
HapMap	African	Sub	222	A=0.059	G=0.941
HapMap	American	Sub	216	A=0.032	G=0.968
Northern Sweden	ACPOP	Study-wide	600	A=0.063	G=0.937
SGDP_PRJ	Global	Study-wide	556	A=0.054	G=0.946
Qatari	Global	Study-wide	216	A=0.028	G=0.972
A Vietnamese Genetic Variation Database	Global	Study-wide	216	A=0.032	G=0.968
Siberian	Global	Study-wide	56	A=0.02	G=0.98
The Danish reference pan genome	Danish	Study-wide	40	A=0.03	G=0.97

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.3419197A>C
GRCh38.p14 chr 6	NC_000006.12:g.3419197A>G
GRCh38.p14 chr 6	NC_000006.12:g.3419197A>T
GRCh37.p13 chr 6	NC_000006.11:g.3419431A>C
GRCh37.p13 chr 6	NC_000006.11:g.3419431A>G
GRCh37.p13 chr 6	NC_000006.11:g.3419431A>T

Gene: SLC22A23, solute carrier family 22 member 23 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
SLC22A23 transcript variant 3	NM_001286455.1:c.-189-334… NM_001286455.1:c.-189-3342T>G	N/A	Intron Variant
SLC22A23 transcript variant 4	NM_001286456.2:c.655-3342… NM_001286456.2:c.655-3342T>G	N/A	Intron Variant
SLC22A23 transcript variant 6	NM_001382317.1:c.655-3342… NM_001382317.1:c.655-3342T>G	N/A	Intron Variant
SLC22A23 transcript variant 9	NM_001382320.1:c.654+3670… NM_001382320.1:c.654+36709T>G	N/A	Intron Variant
SLC22A23 transcript variant 1	NM_015482.2:c.655-3342T>G	N/A	Intron Variant
SLC22A23 transcript variant 2	NM_021945.6:c.-189-3342T>G	N/A	Intron Variant
SLC22A23 transcript variant 7	NM_001382318.1:c.	N/A	Genic Upstream Transcript Variant
SLC22A23 transcript variant 8	NM_001382319.1:c.	N/A	Genic Upstream Transcript Variant
SLC22A23 transcript variant 10	NM_001382321.1:c.	N/A	Genic Upstream Transcript Variant
SLC22A23 transcript variant 5	NR_104448.1:n.	N/A	Intron Variant
SLC22A23 transcript variant 11	NR_168069.1:n.	N/A	Intron Variant
SLC22A23 transcript variant X1	XM_011514801.3:c.727-3342… XM_011514801.3:c.727-3342T>G	N/A	Intron Variant
SLC22A23 transcript variant X5	XM_017011180.2:c.133-3342… XM_017011180.2:c.133-3342T>G	N/A	Intron Variant
SLC22A23 transcript variant X3	XM_017011183.2:c.727-3342… XM_017011183.2:c.727-3342T>G	N/A	Intron Variant
SLC22A23 transcript variant X4	XM_017011185.3:c.727-3342… XM_017011185.3:c.727-3342T>G	N/A	Intron Variant
SLC22A23 transcript variant X11	XM_017011186.2:c.-189-334… XM_017011186.2:c.-189-3342T>G	N/A	Intron Variant
SLC22A23 transcript variant X12	XM_047419244.1:c.*13100=	N/A	3 Prime UTR Variant
SLC22A23 transcript variant X7	XM_017011184.2:c.	N/A	Genic Upstream Transcript Variant
SLC22A23 transcript variant X6	XM_047419241.1:c.	N/A	Genic Upstream Transcript Variant
SLC22A23 transcript variant X8	XM_047419242.1:c.	N/A	Genic Upstream Transcript Variant
SLC22A23 transcript variant X9	XM_047419243.1:c.	N/A	Genic Upstream Transcript Variant
SLC22A23 transcript variant X2	XR_001743575.2:n.	N/A	Intron Variant
SLC22A23 transcript variant X10	XR_007059328.1:n.	N/A	Intron Variant

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=	C	G	T
GRCh38.p14 chr 6	NC_000006.12:g.3419197=	NC_000006.12:g.3419197A>C	NC_000006.12:g.3419197A>G	NC_000006.12:g.3419197A>T
GRCh37.p13 chr 6	NC_000006.11:g.3419431=	NC_000006.11:g.3419431A>C	NC_000006.11:g.3419431A>G	NC_000006.11:g.3419431A>T
SLC22A23 transcript variant X12	XM_047419244.1:c.*13100=	XM_047419244.1:c.*13100T>G	XM_047419244.1:c.*13100T>C	XM_047419244.1:c.*13100T>A
SLC22A23 transcript variant 3	NM_001286455.1:c.-189-3342=	NM_001286455.1:c.-189-3342T>G	NM_001286455.1:c.-189-3342T>C	NM_001286455.1:c.-189-3342T>A
SLC22A23 transcript variant 4	NM_001286456.2:c.655-3342=	NM_001286456.2:c.655-3342T>G	NM_001286456.2:c.655-3342T>C	NM_001286456.2:c.655-3342T>A
SLC22A23 transcript variant 6	NM_001382317.1:c.655-3342=	NM_001382317.1:c.655-3342T>G	NM_001382317.1:c.655-3342T>C	NM_001382317.1:c.655-3342T>A
SLC22A23 transcript variant 9	NM_001382320.1:c.654+36709=	NM_001382320.1:c.654+36709T>G	NM_001382320.1:c.654+36709T>C	NM_001382320.1:c.654+36709T>A
SLC22A23 transcript variant 1	NM_015482.1:c.655-3342=	NM_015482.1:c.655-3342T>G	NM_015482.1:c.655-3342T>C	NM_015482.1:c.655-3342T>A
SLC22A23 transcript variant 1	NM_015482.2:c.655-3342=	NM_015482.2:c.655-3342T>G	NM_015482.2:c.655-3342T>C	NM_015482.2:c.655-3342T>A
SLC22A23 transcript variant 2	NM_021945.5:c.-189-3342=	NM_021945.5:c.-189-3342T>G	NM_021945.5:c.-189-3342T>C	NM_021945.5:c.-189-3342T>A
SLC22A23 transcript variant 2	NM_021945.6:c.-189-3342=	NM_021945.6:c.-189-3342T>G	NM_021945.6:c.-189-3342T>C	NM_021945.6:c.-189-3342T>A
SLC22A23 transcript variant X1	XM_005249285.1:c.655-3342=	XM_005249285.1:c.655-3342T>G	XM_005249285.1:c.655-3342T>C	XM_005249285.1:c.655-3342T>A
SLC22A23 transcript variant X2	XM_005249286.1:c.-189-3342=	XM_005249286.1:c.-189-3342T>G	XM_005249286.1:c.-189-3342T>C	XM_005249286.1:c.-189-3342T>A
SLC22A23 transcript variant X1	XM_011514801.3:c.727-3342=	XM_011514801.3:c.727-3342T>G	XM_011514801.3:c.727-3342T>C	XM_011514801.3:c.727-3342T>A
SLC22A23 transcript variant X5	XM_017011180.2:c.133-3342=	XM_017011180.2:c.133-3342T>G	XM_017011180.2:c.133-3342T>C	XM_017011180.2:c.133-3342T>A
SLC22A23 transcript variant X3	XM_017011183.2:c.727-3342=	XM_017011183.2:c.727-3342T>G	XM_017011183.2:c.727-3342T>C	XM_017011183.2:c.727-3342T>A
SLC22A23 transcript variant X4	XM_017011185.3:c.727-3342=	XM_017011185.3:c.727-3342T>G	XM_017011185.3:c.727-3342T>C	XM_017011185.3:c.727-3342T>A
SLC22A23 transcript variant X11	XM_017011186.2:c.-189-3342=	XM_017011186.2:c.-189-3342T>G	XM_017011186.2:c.-189-3342T>C	XM_017011186.2:c.-189-3342T>A

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#.

93 SubSNP, 21 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	BCM_SSAHASNP	ss10300443	Jul 11, 2003 (116)
2	SC_SNP	ss12921566	Dec 05, 2003 (119)
3	SC_SNP	ss15733849	Feb 27, 2004 (120)
4	CSHL-HAPMAP	ss17890743	Feb 27, 2004 (120)
5	SSAHASNP	ss22509096	Apr 05, 2004 (121)
6	AFFY	ss76577827	Dec 06, 2007 (129)
7	HGSV	ss83539046	Dec 14, 2007 (130)
8	HGSV	ss84009853	Dec 14, 2007 (130)
9	HGSV	ss85504236	Dec 14, 2007 (130)
10	BCMHGSC_JDW	ss93371645	Mar 24, 2008 (129)
11	HUMANGENOME_JCVI	ss98361464	Feb 04, 2009 (130)
12	KRIBB_YJKIM	ss104938261	Feb 04, 2009 (130)
13	BGI	ss105975606	Feb 04, 2009 (130)
14	1000GENOMES	ss109703013	Jan 24, 2009 (130)
15	1000GENOMES	ss113811166	Jan 25, 2009 (130)
16	ILLUMINA-UK	ss116275229	Feb 14, 2009 (130)
17	ENSEMBL	ss143132377	Dec 01, 2009 (131)
18	ENSEMBL	ss143692111	Dec 01, 2009 (131)
19	GMI	ss156457890	Dec 01, 2009 (131)
20	COMPLETE_GENOMICS	ss161969696	Jul 04, 2010 (132)
21	COMPLETE_GENOMICS	ss163068731	Jul 04, 2010 (132)
22	COMPLETE_GENOMICS	ss166037893	Jul 04, 2010 (132)
23	BUSHMAN	ss201339251	Jul 04, 2010 (132)
24	BCM-HGSC-SUB	ss207452329	Jul 04, 2010 (132)
25	1000GENOMES	ss222173439	Jul 14, 2010 (132)
26	1000GENOMES	ss233298005	Jul 14, 2010 (132)
27	1000GENOMES	ss240389120	Jul 15, 2010 (132)
28	BL	ss253993182	May 09, 2011 (134)
29	GMI	ss278628368	May 04, 2012 (137)
30	GMI	ss285327887	Apr 25, 2013 (138)
31	PJP	ss293585972	May 09, 2011 (134)
32	ILLUMINA	ss483539891	May 04, 2012 (137)
33	ILLUMINA	ss485230490	May 04, 2012 (137)
34	ILLUMINA	ss535747143	Sep 08, 2015 (146)
35	TISHKOFF	ss558961579	Apr 25, 2013 (138)
36	SSMP	ss652872814	Apr 25, 2013 (138)
37	ILLUMINA	ss780315816	Aug 21, 2014 (142)
38	ILLUMINA	ss782213490	Aug 21, 2014 (142)
39	ILLUMINA	ss835802866	Aug 21, 2014 (142)
40	EVA-GONL	ss982520011	Aug 21, 2014 (142)
41	JMKIDD_LAB	ss1073332741	Aug 21, 2014 (142)
42	1000GENOMES	ss1318733313	Aug 21, 2014 (142)
43	HAMMER_LAB	ss1397438817	Sep 08, 2015 (146)
44	DDI	ss1430617614	Apr 01, 2015 (144)
45	EVA_GENOME_DK	ss1581506024	Apr 01, 2015 (144)
46	EVA_DECODE	ss1592065855	Apr 01, 2015 (144)
47	EVA_UK10K_ALSPAC	ss1614819388	Apr 01, 2015 (144)
48	EVA_UK10K_TWINSUK	ss1657813421	Apr 01, 2015 (144)
49	HAMMER_LAB	ss1804251063	Sep 08, 2015 (146)
50	WEILL_CORNELL_DGM	ss1925777807	Feb 12, 2016 (147)
51	GENOMED	ss1970295314	Jul 19, 2016 (147)
52	JJLAB	ss2023503403	Sep 14, 2016 (149)
53	USC_VALOUEV	ss2151665364	Dec 20, 2016 (150)
54	HUMAN_LONGEVITY	ss2281301539	Dec 20, 2016 (150)
55	SYSTEMSBIOZJU	ss2626240114	Nov 08, 2017 (151)
56	ILLUMINA	ss2634391126	Nov 08, 2017 (151)
57	GRF	ss2707250491	Nov 08, 2017 (151)
58	GNOMAD	ss2835129377	Nov 08, 2017 (151)
59	SWEGEN	ss2998418194	Nov 08, 2017 (151)
60	BIOINF_KMB_FNS_UNIBA	ss3025535058	Nov 08, 2017 (151)
61	CSHL	ss3346806586	Nov 08, 2017 (151)
62	ILLUMINA	ss3629429211	Oct 12, 2018 (152)
63	ILLUMINA	ss3632311737	Oct 12, 2018 (152)
64	ILLUMINA	ss3642469309	Oct 12, 2018 (152)
65	URBANLAB	ss3648254496	Oct 12, 2018 (152)
66	EGCUT_WGS	ss3666341808	Jul 13, 2019 (153)
67	EVA_DECODE	ss3716462682	Jul 13, 2019 (153)
68	ACPOP	ss3733148837	Jul 13, 2019 (153)
69	EVA	ss3764536948	Jul 13, 2019 (153)
70	PACBIO	ss3785354895	Jul 13, 2019 (153)
71	PACBIO	ss3790722914	Jul 13, 2019 (153)
72	PACBIO	ss3795600075	Jul 13, 2019 (153)
73	KHV_HUMAN_GENOMES	ss3807698150	Jul 13, 2019 (153)
74	EVA	ss3829698960	Apr 26, 2020 (154)
75	EVA	ss3838323861	Apr 26, 2020 (154)
76	EVA	ss3843763689	Apr 26, 2020 (154)
77	SGDP_PRJ	ss3863791792	Apr 26, 2020 (154)
78	KRGDB	ss3910525626	Apr 26, 2020 (154)
79	KOGIC	ss3958383358	Apr 26, 2020 (154)
80	TOPMED	ss4691692625	Apr 26, 2021 (155)
81	TOMMO_GENOMICS	ss5175892129	Apr 26, 2021 (155)
82	1000G_HIGH_COVERAGE	ss5267189526	Oct 13, 2022 (156)
83	EVA	ss5315116721	Oct 13, 2022 (156)
84	EVA	ss5363426768	Oct 13, 2022 (156)
85	HUGCELL_USP	ss5465002817	Oct 13, 2022 (156)
86	1000G_HIGH_COVERAGE	ss5552516309	Oct 13, 2022 (156)
87	SANFORD_IMAGENETICS	ss5639645848	Oct 13, 2022 (156)
88	TOMMO_GENOMICS	ss5713481670	Oct 13, 2022 (156)
89	YY_MCH	ss5807098686	Oct 13, 2022 (156)
90	EVA	ss5841709339	Oct 13, 2022 (156)
91	EVA	ss5855175743	Oct 13, 2022 (156)
92	EVA	ss5882411272	Oct 13, 2022 (156)
93	EVA	ss5968138867	Oct 13, 2022 (156)
94	1000Genomes	NC_000006.11 - 3419431	Oct 12, 2018 (152)
95	1000Genomes_30x	NC_000006.12 - 3419197	Oct 13, 2022 (156)
96	The Avon Longitudinal Study of Parents and Children	NC_000006.11 - 3419431	Oct 12, 2018 (152)
97	Genome-wide autozygosity in Daghestan	NC_000006.10 - 3364430	Apr 26, 2020 (154)
98	Genetic variation in the Estonian population	NC_000006.11 - 3419431	Oct 12, 2018 (152)
99	The Danish reference pan genome	NC_000006.11 - 3419431	Apr 26, 2020 (154)
100	gnomAD - Genomes	NC_000006.12 - 3419197	Apr 26, 2021 (155)
101	Genome of the Netherlands Release 5	NC_000006.11 - 3419431	Apr 26, 2020 (154)
102	HapMap	NC_000006.12 - 3419197	Apr 26, 2020 (154)
103	KOREAN population from KRGDB	NC_000006.11 - 3419431	Apr 26, 2020 (154)
104	Korean Genome Project	NC_000006.12 - 3419197	Apr 26, 2020 (154)
105	Northern Sweden	NC_000006.11 - 3419431	Jul 13, 2019 (153)
106	Qatari	NC_000006.11 - 3419431	Apr 26, 2020 (154)
107	SGDP_PRJ	NC_000006.11 - 3419431	Apr 26, 2020 (154)
108	Siberian	NC_000006.11 - 3419431	Apr 26, 2020 (154)
109	8.3KJPN	NC_000006.11 - 3419431	Apr 26, 2021 (155)
110	14KJPN	NC_000006.12 - 3419197	Oct 13, 2022 (156)
111	TopMed	NC_000006.12 - 3419197	Apr 26, 2021 (155)
112	UK 10K study - Twins	NC_000006.11 - 3419431	Oct 12, 2018 (152)
113	A Vietnamese Genetic Variation Database	NC_000006.11 - 3419431	Jul 13, 2019 (153)
114	ALFA	NC_000006.12 - 3419197	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)
rs57116061	May 23, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
17703020, ss3910525626	NC_000006.11:3419430:A:C	NC_000006.12:3419196:A:C	(self)
ss83539046, ss84009853, ss85504236	NC_000006.9:3364429:A:G	NC_000006.12:3419196:A:G	(self)
413555, ss93371645, ss109703013, ss113811166, ss116275229, ss161969696, ss163068731, ss166037893, ss201339251, ss207452329, ss253993182, ss278628368, ss285327887, ss293585972, ss485230490, ss1397438817, ss1592065855	NC_000006.10:3364429:A:G	NC_000006.12:3419196:A:G	(self)
30466354, 16957426, 12080056, 7670963, 7526730, 17703020, 6433702, 7819737, 15808772, 4181718, 33861436, 16957426, 3755739, ss222173439, ss233298005, ss240389120, ss483539891, ss535747143, ss558961579, ss652872814, ss780315816, ss782213490, ss835802866, ss982520011, ss1073332741, ss1318733313, ss1430617614, ss1581506024, ss1614819388, ss1657813421, ss1804251063, ss1925777807, ss1970295314, ss2023503403, ss2151665364, ss2626240114, ss2634391126, ss2707250491, ss2835129377, ss2998418194, ss3346806586, ss3629429211, ss3632311737, ss3642469309, ss3666341808, ss3733148837, ss3764536948, ss3785354895, ss3790722914, ss3795600075, ss3829698960, ss3838323861, ss3863791792, ss3910525626, ss5175892129, ss5315116721, ss5363426768, ss5639645848, ss5841709339, ss5968138867	NC_000006.11:3419430:A:G	NC_000006.12:3419196:A:G	(self)
40042244, 215422384, 3046644, 14761359, 47318774, 529070183, 5467219379, ss2281301539, ss3025535058, ss3648254496, ss3716462682, ss3807698150, ss3843763689, ss3958383358, ss4691692625, ss5267189526, ss5465002817, ss5552516309, ss5713481670, ss5807098686, ss5855175743, ss5882411272	NC_000006.12:3419196:A:G	NC_000006.12:3419196:A:G	(self)
ss76577827, ss98361464, ss104938261, ss105975606, ss143132377, ss143692111, ss156457890	NT_007592.15:3359430:A:G	NC_000006.12:3419196:A:G	(self)
ss10300443, ss12921566	NT_034880.2:3359429:A:G	NC_000006.12:3419196:A:G	(self)
ss15733849, ss17890743, ss22509096	NT_034880.3:3359429:A:G	NC_000006.12:3419196:A:G	(self)
17703020, ss3910525626	NC_000006.11:3419430:A:T	NC_000006.12:3419196:A:T	(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 rs6915982

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

rs6915982