Name: rs1934953
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.

rs1934953

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr10:95037713 (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: C>A / C>G / C>T
Variation Type: SNV Single Nucleotide Variation
Frequency: C=0.332320 (99107/298228, ALFA)
C=0.315762 (83579/264690, TOPMED)
C=0.307998 (43121/140004, GnomAD) (+ 22 more)
C=0.33547 (26276/78326, PAGE_STUDY)
T=0.48924 (13825/28258, 14KJPN)
T=0.48938 (8202/16760, 8.3KJPN)
C=0.3532 (2262/6404, 1000G_30x)
C=0.3570 (1788/5008, 1000G)
C=0.3623 (1623/4480, Estonian)
C=0.3472 (1338/3854, ALSPAC)
C=0.3355 (1244/3708, TWINSUK)
T=0.4672 (1369/2930, KOREAN)
C=0.3925 (818/2084, HGDP_Stanford)
C=0.3229 (611/1892, HapMap)
T=0.4782 (876/1832, Korea1K)
C=0.372 (371/998, GoNL)
T=0.477 (375/786, PRJEB37584)
T=0.438 (274/626, Chileans)
C=0.410 (246/600, NorthernSweden)
C=0.230 (100/434, SGDP_PRJ)
C=0.245 (53/216, Qatari)
T=0.407 (87/214, Vietnamese)
C=0.06 (4/64, Ancient Sardinia)
C=0.24 (11/46, Siberian)
C=0.47 (19/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: CYP2C8 : Intron Variant
Publications: 3 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	303264	C=0.331869	A=0.000000, T=0.668131
European	Sub	266590	C=0.325620	A=0.000000, T=0.674380
African	Sub	7500	C=0.2027	A=0.0000, T=0.7973
African Others	Sub	280	C=0.207	A=0.000, T=0.793
African American	Sub	7220	C=0.2025	A=0.0000, T=0.7975
Asian	Sub	3894	C=0.4915	A=0.0000, T=0.5085
East Asian	Sub	3138	C=0.5280	A=0.0000, T=0.4720
Other Asian	Sub	756	C=0.340	A=0.000, T=0.660
Latin American 1	Sub	1142	C=0.2671	A=0.0000, T=0.7329
Latin American 2	Sub	8964	C=0.5639	A=0.0000, T=0.4361
South Asian	Sub	5148	C=0.3263	A=0.0000, T=0.6737
Other	Sub	10026	C=0.33543	A=0.00000, T=0.66457

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

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	298228	C=0.332320	A=0.000000, T=0.667680
Allele Frequency Aggregator	European	Sub	263496	C=0.325557	A=0.000000, T=0.674443
Allele Frequency Aggregator	Other	Sub	9226	C=0.3319	A=0.0000, T=0.6681
Allele Frequency Aggregator	Latin American 2	Sub	8964	C=0.5639	A=0.0000, T=0.4361
Allele Frequency Aggregator	African	Sub	6358	C=0.2057	A=0.0000, T=0.7943
Allele Frequency Aggregator	South Asian	Sub	5148	C=0.3263	A=0.0000, T=0.6737
Allele Frequency Aggregator	Asian	Sub	3894	C=0.4915	A=0.0000, T=0.5085
Allele Frequency Aggregator	Latin American 1	Sub	1142	C=0.2671	A=0.0000, T=0.7329
TopMed	Global	Study-wide	264690	C=0.315762	T=0.684238
gnomAD - Genomes	Global	Study-wide	140004	C=0.307998	T=0.692002
gnomAD - Genomes	European	Sub	75822	C=0.33817	T=0.66183
gnomAD - Genomes	African	Sub	41950	C=0.19375	T=0.80625
gnomAD - Genomes	American	Sub	13638	C=0.44002	T=0.55998
gnomAD - Genomes	Ashkenazi Jewish	Sub	3324	C=0.2903	T=0.7097
gnomAD - Genomes	East Asian	Sub	3122	C=0.5448	T=0.4552
gnomAD - Genomes	Other	Sub	2148	C=0.3189	T=0.6811
The PAGE Study	Global	Study-wide	78326	C=0.33547	T=0.66453
The PAGE Study	AfricanAmerican	Sub	32370	C=0.19836	T=0.80164
The PAGE Study	Mexican	Sub	10748	C=0.54810	T=0.45190
The PAGE Study	Asian	Sub	8276	C=0.4959	T=0.5041
The PAGE Study	PuertoRican	Sub	7888	C=0.3181	T=0.6819
The PAGE Study	NativeHawaiian	Sub	4520	C=0.4303	T=0.5697
The PAGE Study	Cuban	Sub	4212	C=0.2785	T=0.7215
The PAGE Study	Dominican	Sub	3802	C=0.2659	T=0.7341
The PAGE Study	CentralAmerican	Sub	2440	C=0.5701	T=0.4299
The PAGE Study	SouthAmerican	Sub	1968	C=0.5361	T=0.4639
The PAGE Study	NativeAmerican	Sub	1252	C=0.4010	T=0.5990
The PAGE Study	SouthAsian	Sub	850	C=0.322	T=0.678
14KJPN	JAPANESE	Study-wide	28258	C=0.51076	T=0.48924
8.3KJPN	JAPANESE	Study-wide	16760	C=0.51062	T=0.48938
1000Genomes_30x	Global	Study-wide	6404	C=0.3532	T=0.6468
1000Genomes_30x	African	Sub	1786	C=0.1937	T=0.8063
1000Genomes_30x	Europe	Sub	1266	C=0.3081	T=0.6919
1000Genomes_30x	South Asian	Sub	1202	C=0.3336	T=0.6664
1000Genomes_30x	East Asian	Sub	1170	C=0.5427	T=0.4573
1000Genomes_30x	American	Sub	980	C=0.500	T=0.500
1000Genomes	Global	Study-wide	5008	C=0.3570	T=0.6430
1000Genomes	African	Sub	1322	C=0.1838	T=0.8162
1000Genomes	East Asian	Sub	1008	C=0.5466	T=0.4534
1000Genomes	Europe	Sub	1006	C=0.3131	T=0.6869
1000Genomes	South Asian	Sub	978	C=0.330	T=0.670
1000Genomes	American	Sub	694	C=0.513	T=0.487
Genetic variation in the Estonian population	Estonian	Study-wide	4480	C=0.3623	T=0.6377
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	C=0.3472	T=0.6528
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	C=0.3355	T=0.6645
KOREAN population from KRGDB	KOREAN	Study-wide	2930	C=0.5328	G=0.0000, T=0.4672
HGDP-CEPH-db Supplement 1	Global	Study-wide	2084	C=0.3925	T=0.6075
HGDP-CEPH-db Supplement 1	Est_Asia	Sub	470	C=0.557	T=0.443
HGDP-CEPH-db Supplement 1	Central_South_Asia	Sub	414	C=0.377	T=0.623
HGDP-CEPH-db Supplement 1	Middle_Est	Sub	350	C=0.169	T=0.831
HGDP-CEPH-db Supplement 1	Europe	Sub	320	C=0.306	T=0.694
HGDP-CEPH-db Supplement 1	Africa	Sub	242	C=0.153	T=0.847
HGDP-CEPH-db Supplement 1	America	Sub	216	C=0.917	T=0.083
HGDP-CEPH-db Supplement 1	Oceania	Sub	72	C=0.11	T=0.89
HapMap	Global	Study-wide	1892	C=0.3229	T=0.6771
HapMap	American	Sub	770	C=0.405	T=0.595
HapMap	African	Sub	692	C=0.175	T=0.825
HapMap	Asian	Sub	254	C=0.524	T=0.476
HapMap	Europe	Sub	176	C=0.256	T=0.744
Korean Genome Project	KOREAN	Study-wide	1832	C=0.5218	T=0.4782
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	C=0.372	T=0.628
CNV burdens in cranial meningiomas	Global	Study-wide	786	C=0.523	T=0.477
CNV burdens in cranial meningiomas	CRM	Sub	786	C=0.523	T=0.477
Chileans	Chilean	Study-wide	626	C=0.562	T=0.438
Northern Sweden	ACPOP	Study-wide	600	C=0.410	T=0.590
SGDP_PRJ	Global	Study-wide	434	C=0.230	T=0.770
Qatari	Global	Study-wide	216	C=0.245	T=0.755
A Vietnamese Genetic Variation Database	Global	Study-wide	214	C=0.593	T=0.407
Ancient Sardinia genome-wide 1240k capture data generation and analysis	Global	Study-wide	64	C=0.06	T=0.94
Siberian	Global	Study-wide	46	C=0.24	T=0.76
The Danish reference pan genome	Danish	Study-wide	40	C=0.47	T=0.53

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 10	NC_000010.11:g.95037713C>A
GRCh38.p14 chr 10	NC_000010.11:g.95037713C>G
GRCh38.p14 chr 10	NC_000010.11:g.95037713C>T
GRCh37.p13 chr 10	NC_000010.10:g.96797470C>A
GRCh37.p13 chr 10	NC_000010.10:g.96797470C>G
GRCh37.p13 chr 10	NC_000010.10:g.96797470C>T
CYP2C8 RefSeqGene	NG_007972.1:g.36785G>T
CYP2C8 RefSeqGene	NG_007972.1:g.36785G>C
CYP2C8 RefSeqGene	NG_007972.1:g.36785G>A

Gene: CYP2C8, cytochrome P450 family 2 subfamily C member 8 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
CYP2C8 transcript variant 1	NM_000770.3:c.1292-404G>T	N/A	Intron Variant
CYP2C8 transcript variant 2	NM_001198853.1:c.1082-404… NM_001198853.1:c.1082-404G>T	N/A	Intron Variant
CYP2C8 transcript variant 3	NM_001198854.1:c.986-404G… NM_001198854.1:c.986-404G>T	N/A	Intron Variant
CYP2C8 transcript variant 4	NM_001198855.1:c.1082-404… NM_001198855.1:c.1082-404G>T	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	C=	A	G	T
GRCh38.p14 chr 10	NC_000010.11:g.95037713=	NC_000010.11:g.95037713C>A	NC_000010.11:g.95037713C>G	NC_000010.11:g.95037713C>T
GRCh37.p13 chr 10	NC_000010.10:g.96797470=	NC_000010.10:g.96797470C>A	NC_000010.10:g.96797470C>G	NC_000010.10:g.96797470C>T
CYP2C8 RefSeqGene	NG_007972.1:g.36785=	NG_007972.1:g.36785G>T	NG_007972.1:g.36785G>C	NG_007972.1:g.36785G>A
CYP2C8 transcript variant 1	NM_000770.3:c.1292-404=	NM_000770.3:c.1292-404G>T	NM_000770.3:c.1292-404G>C	NM_000770.3:c.1292-404G>A
CYP2C8 transcript variant 2	NM_001198853.1:c.1082-404=	NM_001198853.1:c.1082-404G>T	NM_001198853.1:c.1082-404G>C	NM_001198853.1:c.1082-404G>A
CYP2C8 transcript variant 3	NM_001198854.1:c.986-404=	NM_001198854.1:c.986-404G>T	NM_001198854.1:c.986-404G>C	NM_001198854.1:c.986-404G>A
CYP2C8 transcript variant 4	NM_001198855.1:c.1082-404=	NM_001198855.1:c.1082-404G>T	NM_001198855.1:c.1082-404G>C	NM_001198855.1:c.1082-404G>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#.

143 SubSNP, 25 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	TSC-CSHL	ss2824120	Jan 12, 2001 (92)
2	EGP_SNPS	ss16356504	Feb 27, 2004 (120)
3	SSAHASNP	ss20656194	Apr 05, 2004 (121)
4	PERLEGEN	ss24092561	Sep 20, 2004 (123)
5	ABI	ss38533529	Mar 15, 2006 (126)
6	AFFY	ss66373859	Nov 30, 2006 (127)
7	ILLUMINA	ss66578668	Nov 30, 2006 (127)
8	EGP_SNPS	ss66862312	Nov 30, 2006 (127)
9	ILLUMINA	ss67208159	Nov 30, 2006 (127)
10	ILLUMINA	ss67600929	Nov 30, 2006 (127)
11	ILLUMINA	ss70686412	May 26, 2008 (130)
12	ILLUMINA	ss71250796	May 17, 2007 (127)
13	ILLUMINA	ss74920461	Dec 07, 2007 (129)
14	AFFY	ss76102438	Dec 07, 2007 (129)
15	HGSV	ss78156072	Dec 07, 2007 (129)
16	ILLUMINA	ss79102180	Dec 15, 2007 (130)
17	HGSV	ss82567807	Dec 15, 2007 (130)
18	KRIBB_YJKIM	ss83921059	Dec 15, 2007 (130)
19	HUMANGENOME_JCVI	ss97576671	Feb 06, 2009 (130)
20	1000GENOMES	ss113674192	Jan 25, 2009 (130)
21	ILLUMINA-UK	ss119275998	Feb 15, 2009 (130)
22	ILLUMINA	ss121856397	Dec 01, 2009 (131)
23	ENSEMBL	ss137887702	Dec 01, 2009 (131)
24	ILLUMINA	ss153785079	Dec 01, 2009 (131)
25	ILLUMINA	ss159341482	Dec 01, 2009 (131)
26	ILLUMINA	ss160478357	Dec 01, 2009 (131)
27	COMPLETE_GENOMICS	ss168688764	Jul 04, 2010 (132)
28	COMPLETE_GENOMICS	ss170778506	Jul 04, 2010 (132)
29	ILLUMINA	ss170891389	Jul 04, 2010 (132)
30	AFFY	ss172512994	Jul 04, 2010 (132)
31	ILLUMINA	ss172996314	Jul 04, 2010 (132)
32	COMPLETE_GENOMICS	ss174703647	Jul 04, 2010 (132)
33	BUSHMAN	ss201888011	Jul 04, 2010 (132)
34	BCM-HGSC-SUB	ss207048137	Jul 04, 2010 (132)
35	1000GENOMES	ss210770419	Jul 14, 2010 (132)
36	1000GENOMES	ss224884945	Jul 14, 2010 (132)
37	1000GENOMES	ss235293336	Jul 15, 2010 (132)
38	1000GENOMES	ss241976382	Jul 15, 2010 (132)
39	BL	ss254536024	May 09, 2011 (134)
40	GMI	ss280733060	May 04, 2012 (137)
41	GMI	ss286244040	Apr 25, 2013 (138)
42	PJP	ss290909563	May 09, 2011 (134)
43	ILLUMINA	ss480349406	May 04, 2012 (137)
44	ILLUMINA	ss480361311	May 04, 2012 (137)
45	ILLUMINA	ss481128821	Sep 08, 2015 (146)
46	ILLUMINA	ss484972340	May 04, 2012 (137)
47	ILLUMINA	ss537010883	Sep 08, 2015 (146)
48	TISHKOFF	ss562143819	Apr 25, 2013 (138)
49	SSMP	ss657186873	Apr 25, 2013 (138)
50	ILLUMINA	ss779037145	Sep 08, 2015 (146)
51	ILLUMINA	ss782932466	Sep 08, 2015 (146)
52	ILLUMINA	ss783895244	Sep 08, 2015 (146)
53	ILLUMINA	ss825432698	Jul 19, 2016 (147)
54	ILLUMINA	ss832187912	Sep 08, 2015 (146)
55	ILLUMINA	ss832853452	Jul 13, 2019 (153)
56	ILLUMINA	ss834499935	Sep 08, 2015 (146)
57	EVA-GONL	ss987806893	Aug 21, 2014 (142)
58	JMKIDD_LAB	ss1077217172	Aug 21, 2014 (142)
59	1000GENOMES	ss1338633123	Aug 21, 2014 (142)
60	DDI	ss1426411672	Apr 01, 2015 (144)
61	EVA_GENOME_DK	ss1575297611	Apr 01, 2015 (144)
62	EVA_DECODE	ss1597480182	Apr 01, 2015 (144)
63	EVA_UK10K_ALSPAC	ss1625200534	Apr 01, 2015 (144)
64	EVA_UK10K_TWINSUK	ss1668194567	Apr 01, 2015 (144)
65	EVA_SVP	ss1713202780	Apr 01, 2015 (144)
66	ILLUMINA	ss1751988442	Sep 08, 2015 (146)
67	HAMMER_LAB	ss1806520947	Sep 08, 2015 (146)
68	WEILL_CORNELL_DGM	ss1931173026	Feb 12, 2016 (147)
69	ILLUMINA	ss1946289841	Feb 12, 2016 (147)
70	ILLUMINA	ss1959285105	Feb 12, 2016 (147)
71	GENOMED	ss1967200029	Jul 19, 2016 (147)
72	JJLAB	ss2026314719	Sep 14, 2016 (149)
73	USC_VALOUEV	ss2154591484	Nov 08, 2017 (151)
74	HUMAN_LONGEVITY	ss2177164678	Dec 20, 2016 (150)
75	SYSTEMSBIOZJU	ss2627626207	Nov 08, 2017 (151)
76	ILLUMINA	ss2632748620	Nov 08, 2017 (151)
77	GRF	ss2698844354	Nov 08, 2017 (151)
78	ILLUMINA	ss2710717642	Nov 08, 2017 (151)
79	GNOMAD	ss2892154001	Nov 08, 2017 (151)
80	SWEGEN	ss3006969964	Nov 08, 2017 (151)
81	ILLUMINA	ss3021265004	Nov 08, 2017 (151)
82	BIOINF_KMB_FNS_UNIBA	ss3026947452	Nov 08, 2017 (151)
83	CSHL	ss3349262273	Nov 08, 2017 (151)
84	ILLUMINA	ss3625585008	Oct 12, 2018 (152)
85	ILLUMINA	ss3626510229	Oct 12, 2018 (152)
86	ILLUMINA	ss3630771830	Oct 12, 2018 (152)
87	ILLUMINA	ss3632960449	Oct 12, 2018 (152)
88	ILLUMINA	ss3633658101	Oct 12, 2018 (152)
89	ILLUMINA	ss3634417977	Oct 12, 2018 (152)
90	ILLUMINA	ss3635350368	Oct 12, 2018 (152)
91	ILLUMINA	ss3636102610	Oct 12, 2018 (152)
92	ILLUMINA	ss3637101078	Oct 12, 2018 (152)
93	ILLUMINA	ss3637867418	Oct 12, 2018 (152)
94	ILLUMINA	ss3638949455	Oct 12, 2018 (152)
95	ILLUMINA	ss3639474788	Oct 12, 2018 (152)
96	ILLUMINA	ss3640125318	Oct 12, 2018 (152)
97	ILLUMINA	ss3641005388	Oct 12, 2018 (152)
98	ILLUMINA	ss3641299723	Oct 12, 2018 (152)
99	ILLUMINA	ss3642869478	Oct 12, 2018 (152)
100	ILLUMINA	ss3644542587	Oct 12, 2018 (152)
101	URBANLAB	ss3649442017	Oct 12, 2018 (152)
102	ILLUMINA	ss3651623430	Oct 12, 2018 (152)
103	EGCUT_WGS	ss3674381663	Jul 13, 2019 (153)
104	EVA_DECODE	ss3690465998	Jul 13, 2019 (153)
105	ILLUMINA	ss3725179592	Jul 13, 2019 (153)
106	ACPOP	ss3737587437	Jul 13, 2019 (153)
107	ILLUMINA	ss3744074697	Jul 13, 2019 (153)
108	ILLUMINA	ss3744718945	Jul 13, 2019 (153)
109	EVA	ss3748471090	Jul 13, 2019 (153)
110	PAGE_CC	ss3771575773	Jul 13, 2019 (153)
111	ILLUMINA	ss3772219301	Jul 13, 2019 (153)
112	PACBIO	ss3786757207	Jul 13, 2019 (153)
113	PACBIO	ss3791924555	Jul 13, 2019 (153)
114	PACBIO	ss3796806668	Jul 13, 2019 (153)
115	KHV_HUMAN_GENOMES	ss3813837589	Jul 13, 2019 (153)
116	EVA	ss3832277620	Apr 26, 2020 (154)
117	EVA	ss3839680042	Apr 26, 2020 (154)
118	EVA	ss3845153723	Apr 26, 2020 (154)
119	HGDP	ss3847396082	Apr 26, 2020 (154)
120	SGDP_PRJ	ss3874832388	Apr 26, 2020 (154)
121	KRGDB	ss3922961274	Apr 26, 2020 (154)
122	KOGIC	ss3968462531	Apr 26, 2020 (154)
123	EVA	ss3984639080	Apr 26, 2021 (155)
124	EVA	ss3985493344	Apr 26, 2021 (155)
125	TOPMED	ss4862708518	Apr 26, 2021 (155)
126	TOMMO_GENOMICS	ss5198979107	Apr 26, 2021 (155)
127	1000G_HIGH_COVERAGE	ss5285095947	Oct 16, 2022 (156)
128	EVA	ss5315494623	Oct 16, 2022 (156)
129	EVA	ss5395335935	Oct 16, 2022 (156)
130	HUGCELL_USP	ss5480554071	Oct 16, 2022 (156)
131	EVA	ss5510130454	Oct 16, 2022 (156)
132	1000G_HIGH_COVERAGE	ss5579577378	Oct 16, 2022 (156)
133	SANFORD_IMAGENETICS	ss5624255762	Oct 16, 2022 (156)
134	SANFORD_IMAGENETICS	ss5649890594	Oct 16, 2022 (156)
135	TOMMO_GENOMICS	ss5745200156	Oct 16, 2022 (156)
136	EVA	ss5799821614	Oct 16, 2022 (156)
137	YY_MCH	ss5811794389	Oct 16, 2022 (156)
138	EVA	ss5824810214	Oct 16, 2022 (156)
139	EVA	ss5847605699	Oct 16, 2022 (156)
140	EVA	ss5849697860	Oct 16, 2022 (156)
141	EVA	ss5880094543	Oct 16, 2022 (156)
142	EVA	ss5941176967	Oct 16, 2022 (156)
143	EVA	ss5980631542	Oct 16, 2022 (156)
144	1000Genomes	NC_000010.10 - 96797470	Oct 12, 2018 (152)
145	1000Genomes_30x	NC_000010.11 - 95037713	Oct 16, 2022 (156)
146	The Avon Longitudinal Study of Parents and Children	NC_000010.10 - 96797470	Oct 12, 2018 (152)
147	Chileans	NC_000010.10 - 96797470	Apr 26, 2020 (154)
148	Genetic variation in the Estonian population	NC_000010.10 - 96797470	Oct 12, 2018 (152)
149	The Danish reference pan genome	NC_000010.10 - 96797470	Apr 26, 2020 (154)
150	gnomAD - Genomes	NC_000010.11 - 95037713	Apr 26, 2021 (155)
151	Genome of the Netherlands Release 5	NC_000010.10 - 96797470	Apr 26, 2020 (154)
152	HGDP-CEPH-db Supplement 1	NC_000010.9 - 96787460	Apr 26, 2020 (154)
153	HapMap	NC_000010.11 - 95037713	Apr 26, 2020 (154)
154	KOREAN population from KRGDB	NC_000010.10 - 96797470	Apr 26, 2020 (154)
155	Korean Genome Project	NC_000010.11 - 95037713	Apr 26, 2020 (154)
156	Northern Sweden	NC_000010.10 - 96797470	Jul 13, 2019 (153)
157	The PAGE Study	NC_000010.11 - 95037713	Jul 13, 2019 (153)
158	Ancient Sardinia genome-wide 1240k capture data generation and analysis	NC_000010.10 - 96797470	Apr 26, 2021 (155)
159	CNV burdens in cranial meningiomas	NC_000010.10 - 96797470	Apr 26, 2021 (155)
160	Qatari	NC_000010.10 - 96797470	Apr 26, 2020 (154)
161	SGDP_PRJ	NC_000010.10 - 96797470	Apr 26, 2020 (154)
162	Siberian	NC_000010.10 - 96797470	Apr 26, 2020 (154)
163	8.3KJPN	NC_000010.10 - 96797470	Apr 26, 2021 (155)
164	14KJPN	NC_000010.11 - 95037713	Oct 16, 2022 (156)
165	TopMed	NC_000010.11 - 95037713	Apr 26, 2021 (155)
166	UK 10K study - Twins	NC_000010.10 - 96797470	Oct 12, 2018 (152)
167	A Vietnamese Genetic Variation Database	NC_000010.10 - 96797470	Jul 13, 2019 (153)
168	ALFA	NC_000010.11 - 95037713	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)
rs61047308	May 26, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
10491298795	NC_000010.11:95037712:C:A	NC_000010.11:95037712:C:A	(self)
30138668, ss3922961274	NC_000010.10:96797469:C:G	NC_000010.11:95037712:C:G	(self)
ss78156072, ss82567807, ss3638949455, ss3639474788	NC_000010.8:96787459:C:T	NC_000010.11:95037712:C:T	(self)
73974, ss113674192, ss119275998, ss168688764, ss170778506, ss174703647, ss201888011, ss207048137, ss210770419, ss254536024, ss280733060, ss286244040, ss290909563, ss480349406, ss825432698, ss1597480182, ss1713202780, ss3642869478, ss3847396082	NC_000010.9:96787459:C:T	NC_000010.11:95037712:C:T	(self)
51064825, 28350435, 58390, 20119911, 2283434, 12641690, 30138668, 10872302, 719271, 188546, 13214956, 26849368, 7107838, 56948414, 28350435, 6295469, ss224884945, ss235293336, ss241976382, ss480361311, ss481128821, ss484972340, ss537010883, ss562143819, ss657186873, ss779037145, ss782932466, ss783895244, ss832187912, ss832853452, ss834499935, ss987806893, ss1077217172, ss1338633123, ss1426411672, ss1575297611, ss1625200534, ss1668194567, ss1751988442, ss1806520947, ss1931173026, ss1946289841, ss1959285105, ss1967200029, ss2026314719, ss2154591484, ss2627626207, ss2632748620, ss2698844354, ss2710717642, ss2892154001, ss3006969964, ss3021265004, ss3349262273, ss3625585008, ss3626510229, ss3630771830, ss3632960449, ss3633658101, ss3634417977, ss3635350368, ss3636102610, ss3637101078, ss3637867418, ss3640125318, ss3641005388, ss3641299723, ss3644542587, ss3651623430, ss3674381663, ss3737587437, ss3744074697, ss3744718945, ss3748471090, ss3772219301, ss3786757207, ss3791924555, ss3796806668, ss3832277620, ss3839680042, ss3874832388, ss3922961274, ss3984639080, ss3985493344, ss5198979107, ss5315494623, ss5395335935, ss5510130454, ss5624255762, ss5649890594, ss5799821614, ss5824810214, ss5847605699, ss5941176967, ss5980631542	NC_000010.10:96797469:C:T	NC_000010.11:95037712:C:T	(self)
67103313, 360803407, 468494, 24840532, 797242, 79037260, 78254173, 10491298795, ss2177164678, ss3026947452, ss3649442017, ss3690465998, ss3725179592, ss3771575773, ss3813837589, ss3845153723, ss3968462531, ss4862708518, ss5285095947, ss5480554071, ss5579577378, ss5745200156, ss5811794389, ss5849697860, ss5880094543	NC_000010.11:95037712:C:T	NC_000010.11:95037712:C:T	(self)
ss20656194	NT_030059.11:15545995:C:T	NC_000010.11:95037712:C:T	(self)
ss2824120, ss16356504, ss24092561, ss38533529, ss66373859, ss66578668, ss66862312, ss67208159, ss67600929, ss70686412, ss71250796, ss74920461, ss76102438, ss79102180, ss83921059, ss97576671, ss121856397, ss137887702, ss153785079, ss159341482, ss160478357, ss170891389, ss172512994, ss172996314	NT_030059.13:47601933:C:T	NC_000010.11:95037712:C:T	(self)

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

3 citations for rs1934953

PMID	Title	Author	Year	Journal
19761371	Cytochrome P450 2C8 pharmacogenetics: a review of clinical studies.	Daily EB et al.	2009	Pharmacogenomics
28513222	The contribution of CYP2C gene subfamily involved in epoxygenase pathway of arachidonic acids metabolism to hypertension susceptibility in Russian population.	Polonikov A et al.	2017	Clinical and experimental hypertension (New York, N.Y.
28687336	Polymorphisms of CYP2C8, CYP2C9 and CYP2C19 and risk of coronary heart disease in Russian population.	Polonikov A et al.	2017	Gene

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

Genome context:

Select flank length:

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

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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs1934953