Name: rs12917626
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.

rs12917626

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr16:51211743 (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>G / A>T
Variation Type: SNV Single Nucleotide Variation
Frequency: A=0.236456 (72224/305444, ALFA)
A=0.179372 (47478/264690, TOPMED)
A=0.184860 (25900/140106, GnomAD) (+ 21 more)
A=0.13917 (10893/78272, PAGE_STUDY)
A=0.22726 (6422/28258, 14KJPN)
A=0.23186 (3886/16760, 8.3KJPN)
A=0.1496 (958/6404, 1000G_30x)
A=0.1538 (770/5008, 1000G)
A=0.2455 (1100/4480, Estonian)
A=0.2634 (1015/3854, ALSPAC)
A=0.2454 (910/3708, TWINSUK)
A=0.2522 (739/2930, KOREAN)
A=0.1641 (342/2084, HGDP_Stanford)
A=0.1515 (286/1888, HapMap)
A=0.1781 (202/1134, Daghestan)
A=0.261 (260/998, GoNL)
A=0.225 (178/790, PRJEB37584)
A=0.267 (160/600, NorthernSweden)
A=0.109 (59/540, SGDP_PRJ)
A=0.125 (27/216, Qatari)
A=0.259 (55/212, Vietnamese)
G=0.47 (36/76, Ancient Sardinia)
A=0.11 (6/56, Siberian)
A=0.23 (9/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: None
Publications: 0 citations
Genomic View: See rs on genome

ALFA Allele Frequency
The ALFA project provide aggregate allele frequency from dbGaP. More information is available on the project page including descriptions, data access, and terms of use.

Release Version: 20230706150541

Population	Group	Sample Size	Ref Allele	Alt Allele
Total	Global	310480	A=0.235787	G=0.764213
European	Sub	271438	A=0.248624	G=0.751376
African	Sub	12822	A=0.05498	G=0.94502
African Others	Sub	468	A=0.015	G=0.985
African American	Sub	12354	A=0.05650	G=0.94350
Asian	Sub	3974	A=0.2229	G=0.7771
East Asian	Sub	3200	A=0.2372	G=0.7628
Other Asian	Sub	774	A=0.164	G=0.836
Latin American 1	Sub	1220	A=0.1811	G=0.8189
Latin American 2	Sub	5316	A=0.2306	G=0.7694
South Asian	Sub	5234	A=0.0990	G=0.9010
Other	Sub	10476	A=0.20666	G=0.79334

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	305444	A=0.236456	G=0.763544
Allele Frequency Aggregator	European	Sub	268344	A=0.248651	G=0.751349
Allele Frequency Aggregator	African	Sub	11680	A=0.05557	G=0.94443
Allele Frequency Aggregator	Other	Sub	9676	A=0.2067	G=0.7933
Allele Frequency Aggregator	Latin American 2	Sub	5316	A=0.2306	G=0.7694
Allele Frequency Aggregator	South Asian	Sub	5234	A=0.0990	G=0.9010
Allele Frequency Aggregator	Asian	Sub	3974	A=0.2229	G=0.7771
Allele Frequency Aggregator	Latin American 1	Sub	1220	A=0.1811	G=0.8189
TopMed	Global	Study-wide	264690	A=0.179372	G=0.820628
gnomAD - Genomes	Global	Study-wide	140106	A=0.184860	G=0.815140
gnomAD - Genomes	European	Sub	75844	A=0.25091	G=0.74909
gnomAD - Genomes	African	Sub	42004	A=0.05519	G=0.94481
gnomAD - Genomes	American	Sub	13658	A=0.19102	G=0.80898
gnomAD - Genomes	Ashkenazi Jewish	Sub	3322	A=0.2246	G=0.7754
gnomAD - Genomes	East Asian	Sub	3130	A=0.2508	G=0.7492
gnomAD - Genomes	Other	Sub	2148	A=0.1918	G=0.8082
The PAGE Study	Global	Study-wide	78272	A=0.13917	G=0.86083
The PAGE Study	AfricanAmerican	Sub	32360	A=0.06295	G=0.93705
The PAGE Study	Mexican	Sub	10746	A=0.23125	G=0.76875
The PAGE Study	Asian	Sub	8274	A=0.2312	G=0.7688
The PAGE Study	PuertoRican	Sub	7870	A=0.1489	G=0.8511
The PAGE Study	NativeHawaiian	Sub	4512	A=0.2145	G=0.7855
The PAGE Study	Cuban	Sub	4200	A=0.1750	G=0.8250
The PAGE Study	Dominican	Sub	3798	A=0.1130	G=0.8870
The PAGE Study	CentralAmerican	Sub	2438	A=0.1760	G=0.8240
The PAGE Study	SouthAmerican	Sub	1976	A=0.1776	G=0.8224
The PAGE Study	NativeAmerican	Sub	1250	A=0.2304	G=0.7696
The PAGE Study	SouthAsian	Sub	848	A=0.101	G=0.899
14KJPN	JAPANESE	Study-wide	28258	A=0.22726	G=0.77274
8.3KJPN	JAPANESE	Study-wide	16760	A=0.23186	G=0.76814
1000Genomes_30x	Global	Study-wide	6404	A=0.1496	G=0.8504
1000Genomes_30x	African	Sub	1786	A=0.0319	G=0.9681
1000Genomes_30x	Europe	Sub	1266	A=0.2393	G=0.7607
1000Genomes_30x	South Asian	Sub	1202	A=0.0932	G=0.9068
1000Genomes_30x	East Asian	Sub	1170	A=0.2573	G=0.7427
1000Genomes_30x	American	Sub	980	A=0.189	G=0.811
1000Genomes	Global	Study-wide	5008	A=0.1538	G=0.8462
1000Genomes	African	Sub	1322	A=0.0333	G=0.9667
1000Genomes	East Asian	Sub	1008	A=0.2540	G=0.7460
1000Genomes	Europe	Sub	1006	A=0.2416	G=0.7584
1000Genomes	South Asian	Sub	978	A=0.094	G=0.906
1000Genomes	American	Sub	694	A=0.195	G=0.805
Genetic variation in the Estonian population	Estonian	Study-wide	4480	A=0.2455	G=0.7545
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	A=0.2634	G=0.7366
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	A=0.2454	G=0.7546
KOREAN population from KRGDB	KOREAN	Study-wide	2930	A=0.2522	G=0.7478, T=0.0000
HGDP-CEPH-db Supplement 1	Global	Study-wide	2084	A=0.1641	G=0.8359
HGDP-CEPH-db Supplement 1	Est_Asia	Sub	470	A=0.268	G=0.732
HGDP-CEPH-db Supplement 1	Central_South_Asia	Sub	414	A=0.135	G=0.865
HGDP-CEPH-db Supplement 1	Middle_Est	Sub	350	A=0.143	G=0.857
HGDP-CEPH-db Supplement 1	Europe	Sub	320	A=0.216	G=0.784
HGDP-CEPH-db Supplement 1	Africa	Sub	242	A=0.004	G=0.996
HGDP-CEPH-db Supplement 1	America	Sub	216	A=0.176	G=0.824
HGDP-CEPH-db Supplement 1	Oceania	Sub	72	A=0.03	G=0.97
HapMap	Global	Study-wide	1888	A=0.1515	G=0.8485
HapMap	American	Sub	766	A=0.192	G=0.808
HapMap	African	Sub	692	A=0.036	G=0.964
HapMap	Asian	Sub	254	A=0.244	G=0.756
HapMap	Europe	Sub	176	A=0.295	G=0.705
Genome-wide autozygosity in Daghestan	Global	Study-wide	1134	A=0.1781	G=0.8219
Genome-wide autozygosity in Daghestan	Daghestan	Sub	628	A=0.193	G=0.807
Genome-wide autozygosity in Daghestan	Near_East	Sub	144	A=0.201	G=0.799
Genome-wide autozygosity in Daghestan	Central Asia	Sub	120	A=0.158	G=0.842
Genome-wide autozygosity in Daghestan	Europe	Sub	108	A=0.222	G=0.778
Genome-wide autozygosity in Daghestan	South Asian	Sub	98	A=0.07	G=0.93
Genome-wide autozygosity in Daghestan	Caucasus	Sub	36	A=0.06	G=0.94
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	A=0.261	G=0.739
CNV burdens in cranial meningiomas	Global	Study-wide	790	A=0.225	G=0.775
CNV burdens in cranial meningiomas	CRM	Sub	790	A=0.225	G=0.775
Northern Sweden	ACPOP	Study-wide	600	A=0.267	G=0.733
SGDP_PRJ	Global	Study-wide	540	A=0.109	G=0.891
Qatari	Global	Study-wide	216	A=0.125	G=0.875
A Vietnamese Genetic Variation Database	Global	Study-wide	212	A=0.259	G=0.741
Ancient Sardinia genome-wide 1240k capture data generation and analysis	Global	Study-wide	76	A=0.53	G=0.47
Siberian	Global	Study-wide	56	A=0.11	G=0.89
The Danish reference pan genome	Danish	Study-wide	40	A=0.23	G=0.78

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 16	NC_000016.10:g.51211743A>G
GRCh38.p14 chr 16	NC_000016.10:g.51211743A>T
GRCh37.p13 chr 16	NC_000016.9:g.51245654A>G
GRCh37.p13 chr 16	NC_000016.9:g.51245654A>T

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=	G	T
GRCh38.p14 chr 16	NC_000016.10:g.51211743=	NC_000016.10:g.51211743A>G	NC_000016.10:g.51211743A>T
GRCh37.p13 chr 16	NC_000016.9:g.51245654=	NC_000016.9:g.51245654A>G	NC_000016.9:g.51245654A>T

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#.

132 SubSNP, 24 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	SSAHASNP	ss21300553	Apr 05, 2004 (121)
2	ILLUMINA	ss67046501	Dec 01, 2006 (127)
3	ILLUMINA	ss67371976	Dec 01, 2006 (127)
4	ILLUMINA	ss68141239	Dec 12, 2006 (127)
5	ILLUMINA	ss70588505	May 25, 2008 (130)
6	ILLUMINA	ss71131797	May 17, 2007 (127)
7	ILLUMINA	ss75516936	Dec 06, 2007 (129)
8	AFFY	ss76665799	Dec 06, 2007 (129)
9	KRIBB_YJKIM	ss85283929	Dec 15, 2007 (130)
10	BCMHGSC_JDW	ss90390574	Mar 24, 2008 (129)
11	HUMANGENOME_JCVI	ss96635943	Feb 05, 2009 (130)
12	BGI	ss106470980	Feb 05, 2009 (130)
13	1000GENOMES	ss109317885	Jan 23, 2009 (130)
14	1000GENOMES	ss115076326	Jan 25, 2009 (130)
15	ILLUMINA-UK	ss118250039	Feb 14, 2009 (130)
16	ENSEMBL	ss136720176	Dec 01, 2009 (131)
17	ENSEMBL	ss136739334	Dec 01, 2009 (131)
18	ILLUMINA	ss153295227	Dec 01, 2009 (131)
19	ILLUMINA	ss159238804	Dec 01, 2009 (131)
20	ILLUMINA	ss160306714	Dec 01, 2009 (131)
21	COMPLETE_GENOMICS	ss168200558	Jul 04, 2010 (132)
22	COMPLETE_GENOMICS	ss169704899	Jul 04, 2010 (132)
23	COMPLETE_GENOMICS	ss171243432	Jul 04, 2010 (132)
24	ILLUMINA	ss172276844	Jul 04, 2010 (132)
25	BUSHMAN	ss201685387	Jul 04, 2010 (132)
26	BCM-HGSC-SUB	ss207475631	Jul 04, 2010 (132)
27	1000GENOMES	ss227237470	Jul 14, 2010 (132)
28	1000GENOMES	ss237022080	Jul 15, 2010 (132)
29	1000GENOMES	ss243361703	Jul 15, 2010 (132)
30	BL	ss255697173	May 09, 2011 (134)
31	GMI	ss282529169	May 04, 2012 (137)
32	PJP	ss291842070	May 09, 2011 (134)
33	ILLUMINA	ss479841259	May 04, 2012 (137)
34	ILLUMINA	ss479848736	May 04, 2012 (137)
35	ILLUMINA	ss480443567	Sep 08, 2015 (146)
36	ILLUMINA	ss484719116	May 04, 2012 (137)
37	ILLUMINA	ss536821711	Sep 08, 2015 (146)
38	TISHKOFF	ss564895137	Apr 25, 2013 (138)
39	SSMP	ss660666274	Apr 25, 2013 (138)
40	ILLUMINA	ss778792472	Sep 08, 2015 (146)
41	ILLUMINA	ss782806280	Sep 08, 2015 (146)
42	ILLUMINA	ss783771657	Sep 08, 2015 (146)
43	ILLUMINA	ss832059392	Sep 08, 2015 (146)
44	ILLUMINA	ss832751126	Jul 13, 2019 (153)
45	ILLUMINA	ss834252535	Sep 08, 2015 (146)
46	EVA-GONL	ss992481301	Aug 21, 2014 (142)
47	JMKIDD_LAB	ss1080616180	Aug 21, 2014 (142)
48	1000GENOMES	ss1356217051	Aug 21, 2014 (142)
49	HAMMER_LAB	ss1397715016	Sep 08, 2015 (146)
50	DDI	ss1427844906	Apr 01, 2015 (144)
51	EVA_GENOME_DK	ss1577910504	Apr 01, 2015 (144)
52	EVA_UK10K_ALSPAC	ss1634405653	Apr 01, 2015 (144)
53	EVA_UK10K_TWINSUK	ss1677399686	Apr 01, 2015 (144)
54	EVA_DECODE	ss1696514702	Apr 01, 2015 (144)
55	EVA_SVP	ss1713538375	Apr 01, 2015 (144)
56	ILLUMINA	ss1752193642	Sep 08, 2015 (146)
57	HAMMER_LAB	ss1808510584	Sep 08, 2015 (146)
58	WEILL_CORNELL_DGM	ss1935917089	Feb 12, 2016 (147)
59	ILLUMINA	ss1946414710	Feb 12, 2016 (147)
60	ILLUMINA	ss1959677775	Feb 12, 2016 (147)
61	GENOMED	ss1968259166	Jul 19, 2016 (147)
62	JJLAB	ss2028740352	Sep 14, 2016 (149)
63	USC_VALOUEV	ss2157176320	Dec 20, 2016 (150)
64	HUMAN_LONGEVITY	ss2212099257	Dec 20, 2016 (150)
65	SYSTEMSBIOZJU	ss2628861903	Nov 08, 2017 (151)
66	ILLUMINA	ss2633316587	Nov 08, 2017 (151)
67	GRF	ss2701699311	Nov 08, 2017 (151)
68	ILLUMINA	ss2710831935	Nov 08, 2017 (151)
69	GNOMAD	ss2942940634	Nov 08, 2017 (151)
70	SWEGEN	ss3014503703	Nov 08, 2017 (151)
71	ILLUMINA	ss3021705133	Nov 08, 2017 (151)
72	BIOINF_KMB_FNS_UNIBA	ss3028188813	Nov 08, 2017 (151)
73	CSHL	ss3351448624	Nov 08, 2017 (151)
74	ILLUMINA	ss3625692787	Oct 12, 2018 (152)
75	ILLUMINA	ss3627520987	Oct 12, 2018 (152)
76	ILLUMINA	ss3631303058	Oct 12, 2018 (152)
77	ILLUMINA	ss3633120250	Oct 12, 2018 (152)
78	ILLUMINA	ss3633826305	Oct 12, 2018 (152)
79	ILLUMINA	ss3634641596	Oct 12, 2018 (152)
80	ILLUMINA	ss3635514618	Oct 12, 2018 (152)
81	ILLUMINA	ss3636332597	Oct 12, 2018 (152)
82	ILLUMINA	ss3637266049	Oct 12, 2018 (152)
83	ILLUMINA	ss3638124619	Oct 12, 2018 (152)
84	ILLUMINA	ss3639073602	Oct 12, 2018 (152)
85	ILLUMINA	ss3639845647	Oct 12, 2018 (152)
86	ILLUMINA	ss3640348915	Oct 12, 2018 (152)
87	ILLUMINA	ss3643105889	Oct 12, 2018 (152)
88	ILLUMINA	ss3643895444	Oct 12, 2018 (152)
89	ILLUMINA	ss3644667782	Oct 12, 2018 (152)
90	URBANLAB	ss3650508965	Oct 12, 2018 (152)
91	ILLUMINA	ss3652113797	Oct 12, 2018 (152)
92	EGCUT_WGS	ss3681477908	Jul 13, 2019 (153)
93	EVA_DECODE	ss3699249611	Jul 13, 2019 (153)
94	ILLUMINA	ss3725561041	Jul 13, 2019 (153)
95	ACPOP	ss3741504936	Jul 13, 2019 (153)
96	ILLUMINA	ss3744141016	Jul 13, 2019 (153)
97	ILLUMINA	ss3744942018	Jul 13, 2019 (153)
98	EVA	ss3753927650	Jul 13, 2019 (153)
99	PAGE_CC	ss3771878708	Jul 13, 2019 (153)
100	ILLUMINA	ss3772440307	Jul 13, 2019 (153)
101	PACBIO	ss3788037859	Jul 13, 2019 (153)
102	PACBIO	ss3793020854	Jul 13, 2019 (153)
103	PACBIO	ss3797905826	Jul 13, 2019 (153)
104	KHV_HUMAN_GENOMES	ss3819216948	Jul 13, 2019 (153)
105	EVA	ss3834566157	Apr 27, 2020 (154)
106	EVA	ss3840888143	Apr 27, 2020 (154)
107	EVA	ss3846379884	Apr 27, 2020 (154)
108	HGDP	ss3847544717	Apr 27, 2020 (154)
109	SGDP_PRJ	ss3884424014	Apr 27, 2020 (154)
110	KRGDB	ss3933908241	Apr 27, 2020 (154)
111	EVA	ss3984712656	Apr 26, 2021 (155)
112	EVA	ss3985756027	Apr 26, 2021 (155)
113	EVA	ss4017735515	Apr 26, 2021 (155)
114	TOPMED	ss5015151021	Apr 26, 2021 (155)
115	TOMMO_GENOMICS	ss5219545156	Apr 26, 2021 (155)
116	1000G_HIGH_COVERAGE	ss5300936588	Oct 16, 2022 (156)
117	EVA	ss5315836925	Oct 16, 2022 (156)
118	EVA	ss5423668554	Oct 16, 2022 (156)
119	HUGCELL_USP	ss5494287942	Oct 16, 2022 (156)
120	EVA	ss5511608507	Oct 16, 2022 (156)
121	1000G_HIGH_COVERAGE	ss5603572618	Oct 16, 2022 (156)
122	SANFORD_IMAGENETICS	ss5624379646	Oct 16, 2022 (156)
123	SANFORD_IMAGENETICS	ss5658890493	Oct 16, 2022 (156)
124	TOMMO_GENOMICS	ss5774548779	Oct 16, 2022 (156)
125	EVA	ss5799957380	Oct 16, 2022 (156)
126	YY_MCH	ss5815967386	Oct 16, 2022 (156)
127	EVA	ss5846399803	Oct 16, 2022 (156)
128	EVA	ss5847462180	Oct 16, 2022 (156)
129	EVA	ss5851562786	Oct 16, 2022 (156)
130	EVA	ss5899070347	Oct 16, 2022 (156)
131	EVA	ss5950279607	Oct 16, 2022 (156)
132	EVA	ss5979484875	Oct 16, 2022 (156)
133	1000Genomes	NC_000016.9 - 51245654	Oct 12, 2018 (152)
134	1000Genomes_30x	NC_000016.10 - 51211743	Oct 16, 2022 (156)
135	The Avon Longitudinal Study of Parents and Children	NC_000016.9 - 51245654	Oct 12, 2018 (152)
136	Genome-wide autozygosity in Daghestan	NC_000016.8 - 49803155	Apr 27, 2020 (154)
137	Genetic variation in the Estonian population	NC_000016.9 - 51245654	Oct 12, 2018 (152)
138	The Danish reference pan genome	NC_000016.9 - 51245654	Apr 27, 2020 (154)
139	gnomAD - Genomes	NC_000016.10 - 51211743	Apr 26, 2021 (155)
140	Genome of the Netherlands Release 5	NC_000016.9 - 51245654	Apr 27, 2020 (154)
141	HGDP-CEPH-db Supplement 1	NC_000016.8 - 49803155	Apr 27, 2020 (154)
142	HapMap	NC_000016.10 - 51211743	Apr 27, 2020 (154)
143	KOREAN population from KRGDB	NC_000016.9 - 51245654	Apr 27, 2020 (154)
144	Northern Sweden	NC_000016.9 - 51245654	Jul 13, 2019 (153)
145	The PAGE Study	NC_000016.10 - 51211743	Jul 13, 2019 (153)
146	Ancient Sardinia genome-wide 1240k capture data generation and analysis	NC_000016.9 - 51245654	Apr 26, 2021 (155)
147	CNV burdens in cranial meningiomas	NC_000016.9 - 51245654	Apr 26, 2021 (155)
148	Qatari	NC_000016.9 - 51245654	Apr 27, 2020 (154)
149	SGDP_PRJ	NC_000016.9 - 51245654	Apr 27, 2020 (154)
150	Siberian	NC_000016.9 - 51245654	Apr 27, 2020 (154)
151	8.3KJPN	NC_000016.9 - 51245654	Apr 26, 2021 (155)
152	14KJPN	NC_000016.10 - 51211743	Oct 16, 2022 (156)
153	TopMed	NC_000016.10 - 51211743	Apr 26, 2021 (155)
154	UK 10K study - Twins	NC_000016.9 - 51245654	Oct 12, 2018 (152)
155	A Vietnamese Genetic Variation Database	NC_000016.9 - 51245654	Jul 13, 2019 (153)
156	ALFA	NC_000016.10 - 51211743	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)
rs59270440	May 25, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
185022, 222609, ss90390574, ss109317885, ss115076326, ss118250039, ss168200558, ss169704899, ss171243432, ss201685387, ss207475631, ss255697173, ss282529169, ss291842070, ss479841259, ss1397715016, ss1696514702, ss1713538375, ss3639073602, ss3639845647, ss3643105889, ss3643895444, ss3847544717	NC_000016.8:49803154:A:G	NC_000016.10:51211742:A:G	(self)
69378525, 38480682, 27216156, 4123163, 17161547, 41085635, 14789801, 981954, 262191, 17959011, 36440994, 9692674, 77514463, 38480682, 8537431, ss227237470, ss237022080, ss243361703, ss479848736, ss480443567, ss484719116, ss536821711, ss564895137, ss660666274, ss778792472, ss782806280, ss783771657, ss832059392, ss832751126, ss834252535, ss992481301, ss1080616180, ss1356217051, ss1427844906, ss1577910504, ss1634405653, ss1677399686, ss1752193642, ss1808510584, ss1935917089, ss1946414710, ss1959677775, ss1968259166, ss2028740352, ss2157176320, ss2628861903, ss2633316587, ss2701699311, ss2710831935, ss2942940634, ss3014503703, ss3021705133, ss3351448624, ss3625692787, ss3627520987, ss3631303058, ss3633120250, ss3633826305, ss3634641596, ss3635514618, ss3636332597, ss3637266049, ss3638124619, ss3640348915, ss3644667782, ss3652113797, ss3681477908, ss3741504936, ss3744141016, ss3744942018, ss3753927650, ss3772440307, ss3788037859, ss3793020854, ss3797905826, ss3834566157, ss3840888143, ss3884424014, ss3933908241, ss3984712656, ss3985756027, ss4017735515, ss5219545156, ss5315836925, ss5423668554, ss5511608507, ss5624379646, ss5658890493, ss5799957380, ss5846399803, ss5847462180, ss5950279607, ss5979484875	NC_000016.9:51245653:A:G	NC_000016.10:51211742:A:G	(self)
91098553, 489390111, 1380729, 1100177, 108385883, 230696682, 10706927116, ss2212099257, ss3028188813, ss3650508965, ss3699249611, ss3725561041, ss3771878708, ss3819216948, ss3846379884, ss5015151021, ss5300936588, ss5494287942, ss5603572618, ss5774548779, ss5815967386, ss5851562786, ss5899070347	NC_000016.10:51211742:A:G	NC_000016.10:51211742:A:G	(self)
ss67046501, ss67371976, ss68141239, ss70588505, ss71131797, ss75516936, ss76665799, ss85283929, ss96635943, ss106470980, ss136720176, ss136739334, ss153295227, ss159238804, ss160306714, ss172276844	NT_010498.15:4859852:A:G	NC_000016.10:51211742:A:G	(self)
ss21300553	NT_010505.14:3354227:A:G	NC_000016.10:51211742:A:G	(self)
41085635, ss3933908241	NC_000016.9:51245653:A:T	NC_000016.10:51211742: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 rs12917626

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.
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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs12917626