Name: rs864916
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.

rs864916

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr12:25930781 (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
Variation Type: SNV Single Nucleotide Variation
Frequency: G=0.138632 (39002/281334, ALFA)
G=0.206056 (54541/264690, TOPMED)
G=0.134370 (27556/205076, GENOGRAPHIC) (+ 23 more)
G=0.198038 (27742/140084, GnomAD)
G=0.25891 (20376/78700, PAGE_STUDY)
G=0.26902 (7602/28258, 14KJPN)
G=0.27172 (4554/16760, 8.3KJPN)
G=0.2149 (1376/6404, 1000G_30x)
G=0.2119 (1061/5008, 1000G)
G=0.1161 (520/4480, Estonian)
G=0.1220 (470/3854, ALSPAC)
G=0.1238 (459/3708, TWINSUK)
G=0.2454 (719/2930, KOREAN)
G=0.1799 (375/2084, HGDP_Stanford)
G=0.2236 (423/1892, HapMap)
G=0.0827 (94/1136, Daghestan)
G=0.115 (115/998, GoNL)
G=0.181 (143/790, PRJEB37584)
G=0.134 (84/626, Chileans)
G=0.157 (94/600, NorthernSweden)
G=0.171 (37/216, Qatari)
G=0.107 (23/214, Vietnamese)
A=0.402 (70/174, SGDP_PRJ)
G=0.15 (6/40, GENOME_DK)
G=0.10 (4/40, Ancient Sardinia)
A=0.46 (12/26, Siberian)

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	281334	A=0.861368	G=0.138632
European	Sub	245276	A=0.873681	G=0.126319
African	Sub	10682	A=0.64164	G=0.35836
African Others	Sub	384	A=0.565	G=0.435
African American	Sub	10298	A=0.64449	G=0.35551
Asian	Sub	3734	A=0.7801	G=0.2199
East Asian	Sub	3022	A=0.7796	G=0.2204
Other Asian	Sub	712	A=0.782	G=0.218
Latin American 1	Sub	1126	A=0.8135	G=0.1865
Latin American 2	Sub	8048	A=0.8370	G=0.1630
South Asian	Sub	5208	A=0.8687	G=0.1313
Other	Sub	7260	A=0.8397	G=0.1603

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	281334	A=0.861368	G=0.138632
Allele Frequency Aggregator	European	Sub	245276	A=0.873681	G=0.126319
Allele Frequency Aggregator	African	Sub	10682	A=0.64164	G=0.35836
Allele Frequency Aggregator	Latin American 2	Sub	8048	A=0.8370	G=0.1630
Allele Frequency Aggregator	Other	Sub	7260	A=0.8397	G=0.1603
Allele Frequency Aggregator	South Asian	Sub	5208	A=0.8687	G=0.1313
Allele Frequency Aggregator	Asian	Sub	3734	A=0.7801	G=0.2199
Allele Frequency Aggregator	Latin American 1	Sub	1126	A=0.8135	G=0.1865
TopMed	Global	Study-wide	264690	A=0.793944	G=0.206056
Genographic Project	Global	Study-wide	205076	A=0.865630	G=0.134370
gnomAD - Genomes	Global	Study-wide	140084	A=0.801962	G=0.198038
gnomAD - Genomes	European	Sub	75914	A=0.88009	G=0.11991
gnomAD - Genomes	African	Sub	41924	A=0.63897	G=0.36103
gnomAD - Genomes	American	Sub	13644	A=0.84352	G=0.15648
gnomAD - Genomes	Ashkenazi Jewish	Sub	3324	A=0.8812	G=0.1188
gnomAD - Genomes	East Asian	Sub	3128	A=0.8136	G=0.1864
gnomAD - Genomes	Other	Sub	2150	A=0.8186	G=0.1814
The PAGE Study	Global	Study-wide	78700	A=0.74109	G=0.25891
The PAGE Study	AfricanAmerican	Sub	32516	A=0.64547	G=0.35453
The PAGE Study	Mexican	Sub	10810	A=0.83349	G=0.16651
The PAGE Study	Asian	Sub	8318	A=0.7460	G=0.2540
The PAGE Study	PuertoRican	Sub	7916	A=0.8254	G=0.1746
The PAGE Study	NativeHawaiian	Sub	4534	A=0.8291	G=0.1709
The PAGE Study	Cuban	Sub	4230	A=0.8340	G=0.1660
The PAGE Study	Dominican	Sub	3828	A=0.7544	G=0.2456
The PAGE Study	CentralAmerican	Sub	2450	A=0.8184	G=0.1816
The PAGE Study	SouthAmerican	Sub	1982	A=0.8300	G=0.1700
The PAGE Study	NativeAmerican	Sub	1260	A=0.8214	G=0.1786
The PAGE Study	SouthAsian	Sub	856	A=0.849	G=0.151
14KJPN	JAPANESE	Study-wide	28258	A=0.73098	G=0.26902
8.3KJPN	JAPANESE	Study-wide	16760	A=0.72828	G=0.27172
1000Genomes_30x	Global	Study-wide	6404	A=0.7851	G=0.2149
1000Genomes_30x	African	Sub	1786	A=0.6271	G=0.3729
1000Genomes_30x	Europe	Sub	1266	A=0.8681	G=0.1319
1000Genomes_30x	South Asian	Sub	1202	A=0.8469	G=0.1531
1000Genomes_30x	East Asian	Sub	1170	A=0.8231	G=0.1769
1000Genomes_30x	American	Sub	980	A=0.845	G=0.155
1000Genomes	Global	Study-wide	5008	A=0.7881	G=0.2119
1000Genomes	African	Sub	1322	A=0.6172	G=0.3828
1000Genomes	East Asian	Sub	1008	A=0.8313	G=0.1687
1000Genomes	Europe	Sub	1006	A=0.8738	G=0.1262
1000Genomes	South Asian	Sub	978	A=0.848	G=0.152
1000Genomes	American	Sub	694	A=0.843	G=0.157
Genetic variation in the Estonian population	Estonian	Study-wide	4480	A=0.8839	G=0.1161
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	A=0.8780	G=0.1220
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	A=0.8762	G=0.1238
KOREAN population from KRGDB	KOREAN	Study-wide	2930	A=0.7546	G=0.2454
HGDP-CEPH-db Supplement 1	Global	Study-wide	2084	A=0.8201	G=0.1799
HGDP-CEPH-db Supplement 1	Est_Asia	Sub	470	A=0.821	G=0.179
HGDP-CEPH-db Supplement 1	Central_South_Asia	Sub	414	A=0.899	G=0.101
HGDP-CEPH-db Supplement 1	Middle_Est	Sub	350	A=0.831	G=0.169
HGDP-CEPH-db Supplement 1	Europe	Sub	320	A=0.869	G=0.131
HGDP-CEPH-db Supplement 1	Africa	Sub	242	A=0.583	G=0.417
HGDP-CEPH-db Supplement 1	America	Sub	216	A=0.861	G=0.139
HGDP-CEPH-db Supplement 1	Oceania	Sub	72	A=0.76	G=0.24
HapMap	Global	Study-wide	1892	A=0.7764	G=0.2236
HapMap	American	Sub	770	A=0.853	G=0.147
HapMap	African	Sub	692	A=0.663	G=0.337
HapMap	Asian	Sub	254	A=0.776	G=0.224
HapMap	Europe	Sub	176	A=0.886	G=0.114
Genome-wide autozygosity in Daghestan	Global	Study-wide	1136	A=0.9173	G=0.0827
Genome-wide autozygosity in Daghestan	Daghestan	Sub	628	A=0.935	G=0.065
Genome-wide autozygosity in Daghestan	Near_East	Sub	144	A=0.910	G=0.090
Genome-wide autozygosity in Daghestan	Central Asia	Sub	122	A=0.893	G=0.107
Genome-wide autozygosity in Daghestan	Europe	Sub	108	A=0.889	G=0.111
Genome-wide autozygosity in Daghestan	South Asian	Sub	98	A=0.88	G=0.12
Genome-wide autozygosity in Daghestan	Caucasus	Sub	36	A=0.92	G=0.08
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	A=0.885	G=0.115
CNV burdens in cranial meningiomas	Global	Study-wide	790	A=0.819	G=0.181
CNV burdens in cranial meningiomas	CRM	Sub	790	A=0.819	G=0.181
Chileans	Chilean	Study-wide	626	A=0.866	G=0.134
Northern Sweden	ACPOP	Study-wide	600	A=0.843	G=0.157
Qatari	Global	Study-wide	216	A=0.829	G=0.171
A Vietnamese Genetic Variation Database	Global	Study-wide	214	A=0.893	G=0.107
SGDP_PRJ	Global	Study-wide	174	A=0.402	G=0.598
The Danish reference pan genome	Danish	Study-wide	40	A=0.85	G=0.15
Ancient Sardinia genome-wide 1240k capture data generation and analysis	Global	Study-wide	40	A=0.90	G=0.10
Siberian	Global	Study-wide	26	A=0.46	G=0.54

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 12	NC_000012.12:g.25930781A>G
GRCh37.p13 chr 12	NC_000012.11:g.26083714A>G

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
GRCh38.p14 chr 12	NC_000012.12:g.25930781=	NC_000012.12:g.25930781A>G
GRCh37.p13 chr 12	NC_000012.11:g.26083714=	NC_000012.11:g.26083714A>G

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#.

122 SubSNP, 26 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	KWOK	ss1282036	Oct 05, 2000 (86)
2	KWOK	ss1635302	Oct 18, 2000 (87)
3	SC_JCM	ss2665515	Nov 09, 2000 (92)
4	CSHL-HAPMAP	ss17472624	Feb 27, 2004 (120)
5	PERLEGEN	ss23429741	Sep 20, 2004 (123)
6	ABI	ss38908511	Mar 15, 2006 (126)
7	AFFY	ss66075688	Dec 01, 2006 (127)
8	ILLUMINA	ss67882466	Dec 01, 2006 (127)
9	ILLUMINA	ss68022853	Dec 01, 2006 (127)
10	ILLUMINA	ss68297602	Dec 12, 2006 (127)
11	PERLEGEN	ss69104634	May 17, 2007 (127)
12	ILLUMINA	ss70975861	May 24, 2008 (130)
13	ILLUMINA	ss71587476	May 17, 2007 (127)
14	ILLUMINA	ss75883378	Dec 06, 2007 (129)
15	AFFY	ss76010772	Dec 08, 2007 (130)
16	KRIBB_YJKIM	ss83583357	Dec 15, 2007 (130)
17	HGSV	ss84074909	Dec 15, 2007 (130)
18	BGI	ss103033685	Dec 01, 2009 (131)
19	1000GENOMES	ss111671452	Jan 25, 2009 (130)
20	1000GENOMES	ss113315169	Jan 25, 2009 (130)
21	ILLUMINA-UK	ss118658298	Feb 14, 2009 (130)
22	ILLUMINA	ss154474968	Dec 01, 2009 (131)
23	ILLUMINA	ss159649449	Dec 01, 2009 (131)
24	ILLUMINA	ss160959409	Dec 01, 2009 (131)
25	ENSEMBL	ss161511905	Dec 01, 2009 (131)
26	COMPLETE_GENOMICS	ss169379854	Jul 04, 2010 (132)
27	AFFY	ss170377817	Jul 04, 2010 (132)
28	ILLUMINA	ss174754476	Jul 04, 2010 (132)
29	BUSHMAN	ss197910116	Jul 04, 2010 (132)
30	1000GENOMES	ss225662669	Jul 14, 2010 (132)
31	1000GENOMES	ss235868181	Jul 15, 2010 (132)
32	1000GENOMES	ss242437707	Jul 15, 2010 (132)
33	GMI	ss281318164	May 04, 2012 (137)
34	PJP	ss291404909	May 09, 2011 (134)
35	ILLUMINA	ss481813665	May 04, 2012 (137)
36	ILLUMINA	ss481846183	May 04, 2012 (137)
37	ILLUMINA	ss482806990	Sep 08, 2015 (146)
38	ILLUMINA	ss485701494	May 04, 2012 (137)
39	TISHKOFF	ss563060881	Apr 25, 2013 (138)
40	SSMP	ss658599552	Apr 25, 2013 (138)
41	ILLUMINA	ss783296312	Aug 21, 2014 (142)
42	ILLUMINA	ss832557621	Apr 01, 2015 (144)
43	ILLUMINA	ss833160265	Aug 21, 2014 (142)
44	ILLUMINA	ss833751093	Aug 21, 2014 (142)
45	EVA-GONL	ss989352713	Aug 21, 2014 (142)
46	JMKIDD_LAB	ss1078332820	Aug 21, 2014 (142)
47	1000GENOMES	ss1344337353	Aug 21, 2014 (142)
48	HAMMER_LAB	ss1397629634	Sep 08, 2015 (146)
49	DDI	ss1426878349	Apr 01, 2015 (144)
50	EVA_GENOME_DK	ss1576176510	Apr 01, 2015 (144)
51	EVA_DECODE	ss1599026737	Apr 01, 2015 (144)
52	EVA_UK10K_ALSPAC	ss1628239428	Apr 01, 2015 (144)
53	EVA_UK10K_TWINSUK	ss1671233461	Apr 01, 2015 (144)
54	EVA_SVP	ss1713315667	Apr 01, 2015 (144)
55	ILLUMINA	ss1752062175	Sep 08, 2015 (146)
56	HAMMER_LAB	ss1807168037	Sep 08, 2015 (146)
57	WEILL_CORNELL_DGM	ss1932716000	Feb 12, 2016 (147)
58	ILLUMINA	ss1946334487	Feb 12, 2016 (147)
59	ILLUMINA	ss1959422438	Feb 12, 2016 (147)
60	GENOMED	ss1967551599	Jul 19, 2016 (147)
61	JJLAB	ss2027106788	Sep 14, 2016 (149)
62	USC_VALOUEV	ss2155433042	Dec 20, 2016 (150)
63	HUMAN_LONGEVITY	ss2188653427	Dec 20, 2016 (150)
64	SYSTEMSBIOZJU	ss2628033360	Nov 08, 2017 (151)
65	ILLUMINA	ss2632939604	Nov 08, 2017 (151)
66	GRF	ss2699762684	Nov 08, 2017 (151)
67	GNOMAD	ss2908554144	Nov 08, 2017 (151)
68	SWEGEN	ss3009385867	Nov 08, 2017 (151)
69	BIOINF_KMB_FNS_UNIBA	ss3027360472	Nov 08, 2017 (151)
70	CSHL	ss3349977733	Nov 08, 2017 (151)
71	ILLUMINA	ss3625618554	Oct 12, 2018 (152)
72	ILLUMINA	ss3633014968	Oct 12, 2018 (152)
73	ILLUMINA	ss3633715647	Oct 12, 2018 (152)
74	ILLUMINA	ss3634496927	Oct 12, 2018 (152)
75	ILLUMINA	ss3635406582	Oct 12, 2018 (152)
76	ILLUMINA	ss3636181478	Oct 12, 2018 (152)
77	ILLUMINA	ss3637157543	Oct 12, 2018 (152)
78	ILLUMINA	ss3637953901	Oct 12, 2018 (152)
79	ILLUMINA	ss3638990929	Oct 12, 2018 (152)
80	ILLUMINA	ss3639806176	Oct 12, 2018 (152)
81	ILLUMINA	ss3640204260	Oct 12, 2018 (152)
82	ILLUMINA	ss3642948307	Oct 12, 2018 (152)
83	ILLUMINA	ss3643857822	Oct 12, 2018 (152)
84	ILLUMINA	ss3644587446	Oct 12, 2018 (152)
85	EGCUT_WGS	ss3676703943	Jul 13, 2019 (153)
86	EVA_DECODE	ss3693326511	Jul 13, 2019 (153)
87	ACPOP	ss3738867122	Jul 13, 2019 (153)
88	ILLUMINA	ss3744096975	Jul 13, 2019 (153)
89	ILLUMINA	ss3744797644	Jul 13, 2019 (153)
90	EVA	ss3750271382	Jul 13, 2019 (153)
91	PAGE_CC	ss3771681538	Jul 13, 2019 (153)
92	ILLUMINA	ss3772297148	Jul 13, 2019 (153)
93	PACBIO	ss3787177240	Jul 13, 2019 (153)
94	PACBIO	ss3792286513	Jul 13, 2019 (153)
95	PACBIO	ss3797169202	Jul 13, 2019 (153)
96	KHV_HUMAN_GENOMES	ss3815590891	Jul 13, 2019 (153)
97	EVA	ss3833033139	Apr 26, 2020 (154)
98	EVA	ss3840084713	Apr 26, 2020 (154)
99	EVA	ss3845568747	Apr 26, 2020 (154)
100	HGDP	ss3847445579	Apr 26, 2020 (154)
101	SGDP_PRJ	ss3877914249	Apr 26, 2020 (154)
102	KRGDB	ss3926453389	Apr 26, 2020 (154)
103	EVA	ss3984664292	Apr 26, 2021 (155)
104	EVA	ss3985581925	Apr 26, 2021 (155)
105	EVA	ss4017580352	Apr 26, 2021 (155)
106	TOPMED	ss4912392965	Apr 26, 2021 (155)
107	TOMMO_GENOMICS	ss5205545490	Apr 26, 2021 (155)
108	1000G_HIGH_COVERAGE	ss5290180699	Oct 16, 2022 (156)
109	GENOGRAPHIC	ss5314550199	Oct 16, 2022 (156)
110	EVA	ss5315609392	Oct 16, 2022 (156)
111	EVA	ss5404592642	Oct 16, 2022 (156)
112	HUGCELL_USP	ss5485030740	Oct 16, 2022 (156)
113	EVA	ss5510629488	Oct 16, 2022 (156)
114	1000G_HIGH_COVERAGE	ss5587295743	Oct 16, 2022 (156)
115	SANFORD_IMAGENETICS	ss5652805946	Oct 16, 2022 (156)
116	TOMMO_GENOMICS	ss5754483000	Oct 16, 2022 (156)
117	YY_MCH	ss5813107903	Oct 16, 2022 (156)
118	EVA	ss5837736449	Oct 16, 2022 (156)
119	EVA	ss5847664118	Oct 16, 2022 (156)
120	EVA	ss5850306284	Oct 16, 2022 (156)
121	EVA	ss5903707205	Oct 16, 2022 (156)
122	EVA	ss5944160003	Oct 16, 2022 (156)
123	1000Genomes	NC_000012.11 - 26083714	Oct 12, 2018 (152)
124	1000Genomes_30x	NC_000012.12 - 25930781	Oct 16, 2022 (156)
125	The Avon Longitudinal Study of Parents and Children	NC_000012.11 - 26083714	Oct 12, 2018 (152)
126	Chileans	NC_000012.11 - 26083714	Apr 26, 2020 (154)
127	Genome-wide autozygosity in Daghestan	NC_000012.10 - 25974981	Apr 26, 2020 (154)
128	Genetic variation in the Estonian population	NC_000012.11 - 26083714	Oct 12, 2018 (152)
129	Genographic Project	NC_000012.12 - 25930781	Oct 16, 2022 (156)
130	The Danish reference pan genome	NC_000012.11 - 26083714	Apr 26, 2020 (154)
131	gnomAD - Genomes	NC_000012.12 - 25930781	Apr 26, 2021 (155)
132	Genome of the Netherlands Release 5	NC_000012.11 - 26083714	Apr 26, 2020 (154)
133	HGDP-CEPH-db Supplement 1	NC_000012.10 - 25974981	Apr 26, 2020 (154)
134	HapMap	NC_000012.12 - 25930781	Apr 26, 2020 (154)
135	KOREAN population from KRGDB	NC_000012.11 - 26083714	Apr 26, 2020 (154)
136	Northern Sweden	NC_000012.11 - 26083714	Jul 13, 2019 (153)
137	The PAGE Study	NC_000012.12 - 25930781	Jul 13, 2019 (153)
138	Ancient Sardinia genome-wide 1240k capture data generation and analysis	NC_000012.11 - 26083714	Apr 26, 2021 (155)
139	CNV burdens in cranial meningiomas	NC_000012.11 - 26083714	Apr 26, 2021 (155)
140	Qatari	NC_000012.11 - 26083714	Apr 26, 2020 (154)
141	SGDP_PRJ	NC_000012.11 - 26083714	Apr 26, 2020 (154)
142	Siberian	NC_000012.11 - 26083714	Apr 26, 2020 (154)
143	8.3KJPN	NC_000012.11 - 26083714	Apr 26, 2021 (155)
144	14KJPN	NC_000012.12 - 25930781	Oct 16, 2022 (156)
145	TopMed	NC_000012.12 - 25930781	Apr 26, 2021 (155)
146	UK 10K study - Twins	NC_000012.11 - 26083714	Oct 12, 2018 (152)
147	A Vietnamese Genetic Variation Database	NC_000012.11 - 26083714	Jul 13, 2019 (153)
148	ALFA	NC_000012.12 - 25930781	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)
rs1797974	Jan 18, 2001 (92)
rs56608182	May 24, 2008 (130)
rs58808730	May 24, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss84074909, ss3638990929, ss3639806176, ss3643857822	NC_000012.9:25974980:A:G	NC_000012.12:25930780:A:G	(self)
100598, 123471, ss66075688, ss76010772, ss111671452, ss113315169, ss118658298, ss160959409, ss169379854, ss170377817, ss197910116, ss281318164, ss291404909, ss481813665, ss1397629634, ss1599026737, ss1713315667, ss3642948307, ss3847445579	NC_000012.10:25974980:A:G	NC_000012.12:25930780:A:G	(self)
57061378, 31687784, 95324, 22442191, 2891200, 14138278, 33630783, 12151987, 807852, 213784, 14757930, 29931229, 7949396, 63514797, 31687784, 7031474, ss225662669, ss235868181, ss242437707, ss481846183, ss482806990, ss485701494, ss563060881, ss658599552, ss783296312, ss832557621, ss833160265, ss833751093, ss989352713, ss1078332820, ss1344337353, ss1426878349, ss1576176510, ss1628239428, ss1671233461, ss1752062175, ss1807168037, ss1932716000, ss1946334487, ss1959422438, ss1967551599, ss2027106788, ss2155433042, ss2628033360, ss2632939604, ss2699762684, ss2908554144, ss3009385867, ss3349977733, ss3625618554, ss3633014968, ss3633715647, ss3634496927, ss3635406582, ss3636181478, ss3637157543, ss3637953901, ss3640204260, ss3644587446, ss3676703943, ss3738867122, ss3744096975, ss3744797644, ss3750271382, ss3772297148, ss3787177240, ss3792286513, ss3797169202, ss3833033139, ss3840084713, ss3877914249, ss3926453389, ss3984664292, ss3985581925, ss4017580352, ss5205545490, ss5315609392, ss5404592642, ss5510629488, ss5652805946, ss5837736449, ss5847664118, ss5944160003	NC_000012.11:26083713:A:G	NC_000012.12:25930780:A:G	(self)
74821678, 80870, 402356301, 779392, 903007, 88320104, 127938622, 13951374672, ss2188653427, ss3027360472, ss3693326511, ss3771681538, ss3815590891, ss3845568747, ss4912392965, ss5290180699, ss5314550199, ss5485030740, ss5587295743, ss5754483000, ss5813107903, ss5850306284, ss5903707205	NC_000012.12:25930780:A:G	NC_000012.12:25930780:A:G	(self)
ss17472624	NT_009714.16:18842687:A:G	NC_000012.12:25930780:A:G	(self)
ss1282036, ss1635302, ss2665515, ss23429741, ss38908511, ss67882466, ss68022853, ss68297602, ss69104634, ss70975861, ss71587476, ss75883378, ss83583357, ss103033685, ss154474968, ss159649449, ss161511905, ss174754476	NT_009714.17:18843837:A:G	NC_000012.12:25930780:A:G	(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 rs864916

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.

Choose placement

dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs864916