Name: rs4961374
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.

rs4961374

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr8:141354063 (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: T>C
Variation Type: SNV Single Nucleotide Variation
Frequency: T=0.228841 (60572/264690, TOPMED)
T=0.243982 (37845/155114, ALFA)
T=0.223518 (31327/140154, GnomAD) (+ 20 more)
T=0.24337 (19152/78696, PAGE_STUDY)
T=0.44929 (12696/28258, 14KJPN)
T=0.44612 (7477/16760, 8.3KJPN)
T=0.2800 (1793/6404, 1000G_30x)
T=0.2861 (1433/5008, 1000G)
T=0.2054 (920/4480, Estonian)
T=0.2436 (939/3854, ALSPAC)
T=0.2500 (927/3708, TWINSUK)
T=0.4331 (1268/2928, KOREAN)
T=0.3208 (668/2082, HGDP_Stanford)
T=0.2748 (520/1892, HapMap)
T=0.239 (239/998, GoNL)
T=0.443 (349/788, PRJEB37584)
T=0.162 (97/600, NorthernSweden)
T=0.232 (116/500, SGDP_PRJ)
T=0.231 (50/216, Qatari)
C=0.463 (100/216, Vietnamese)
T=0.43 (38/88, Ancient Sardinia)
T=0.26 (12/46, Siberian)
T=0.38 (15/40, 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	160148	T=0.243437	C=0.756563
European	Sub	140982	T=0.247230	C=0.752770
African	Sub	5618	T=0.1915	C=0.8085
African Others	Sub	208	T=0.178	C=0.822
African American	Sub	5410	T=0.1921	C=0.8079
Asian	Sub	500	T=0.466	C=0.534
East Asian	Sub	432	T=0.463	C=0.537
Other Asian	Sub	68	T=0.49	C=0.51
Latin American 1	Sub	370	T=0.224	C=0.776
Latin American 2	Sub	5554	T=0.1696	C=0.8304
South Asian	Sub	170	T=0.341	C=0.659
Other	Sub	6954	T=0.2501	C=0.7499

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").

Download

Study	Population	Group	Sample Size	Ref Allele	Alt Allele
TopMed	Global	Study-wide	264690	T=0.228841	C=0.771159
Allele Frequency Aggregator	Total	Global	155114	T=0.243982	C=0.756018
Allele Frequency Aggregator	European	Sub	137890	T=0.247552	C=0.752448
Allele Frequency Aggregator	Other	Sub	6154	T=0.2512	C=0.7488
Allele Frequency Aggregator	Latin American 2	Sub	5554	T=0.1696	C=0.8304
Allele Frequency Aggregator	African	Sub	4476	T=0.1895	C=0.8105
Allele Frequency Aggregator	Asian	Sub	500	T=0.466	C=0.534
Allele Frequency Aggregator	Latin American 1	Sub	370	T=0.224	C=0.776
Allele Frequency Aggregator	South Asian	Sub	170	T=0.341	C=0.659
gnomAD - Genomes	Global	Study-wide	140154	T=0.223518	C=0.776482
gnomAD - Genomes	European	Sub	75912	T=0.23547	C=0.76453
gnomAD - Genomes	African	Sub	41990	T=0.18721	C=0.81279
gnomAD - Genomes	American	Sub	13658	T=0.19366	C=0.80634
gnomAD - Genomes	Ashkenazi Jewish	Sub	3324	T=0.2837	C=0.7163
gnomAD - Genomes	East Asian	Sub	3118	T=0.4702	C=0.5298
gnomAD - Genomes	Other	Sub	2152	T=0.2495	C=0.7505
The PAGE Study	Global	Study-wide	78696	T=0.24337	C=0.75663
The PAGE Study	AfricanAmerican	Sub	32512	T=0.18753	C=0.81247
The PAGE Study	Mexican	Sub	10808	T=0.18570	C=0.81430
The PAGE Study	Asian	Sub	8318	T=0.4542	C=0.5458
The PAGE Study	PuertoRican	Sub	7918	T=0.2189	C=0.7811
The PAGE Study	NativeHawaiian	Sub	4534	T=0.5282	C=0.4718
The PAGE Study	Cuban	Sub	4230	T=0.2423	C=0.7577
The PAGE Study	Dominican	Sub	3828	T=0.2066	C=0.7934
The PAGE Study	CentralAmerican	Sub	2450	T=0.1604	C=0.8396
The PAGE Study	SouthAmerican	Sub	1982	T=0.1736	C=0.8264
The PAGE Study	NativeAmerican	Sub	1260	T=0.2302	C=0.7698
The PAGE Study	SouthAsian	Sub	856	T=0.349	C=0.651
14KJPN	JAPANESE	Study-wide	28258	T=0.44929	C=0.55071
8.3KJPN	JAPANESE	Study-wide	16760	T=0.44612	C=0.55388
1000Genomes_30x	Global	Study-wide	6404	T=0.2800	C=0.7200
1000Genomes_30x	African	Sub	1786	T=0.1915	C=0.8085
1000Genomes_30x	Europe	Sub	1266	T=0.2267	C=0.7733
1000Genomes_30x	South Asian	Sub	1202	T=0.3428	C=0.6572
1000Genomes_30x	East Asian	Sub	1170	T=0.4863	C=0.5137
1000Genomes_30x	American	Sub	980	T=0.187	C=0.813
1000Genomes	Global	Study-wide	5008	T=0.2861	C=0.7139
1000Genomes	African	Sub	1322	T=0.1921	C=0.8079
1000Genomes	East Asian	Sub	1008	T=0.4931	C=0.5069
1000Genomes	Europe	Sub	1006	T=0.2187	C=0.7813
1000Genomes	South Asian	Sub	978	T=0.343	C=0.657
1000Genomes	American	Sub	694	T=0.183	C=0.817
Genetic variation in the Estonian population	Estonian	Study-wide	4480	T=0.2054	C=0.7946
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	T=0.2436	C=0.7564
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	T=0.2500	C=0.7500
KOREAN population from KRGDB	KOREAN	Study-wide	2928	T=0.4331	C=0.5669
HGDP-CEPH-db Supplement 1	Global	Study-wide	2082	T=0.3208	C=0.6792
HGDP-CEPH-db Supplement 1	Est_Asia	Sub	470	T=0.534	C=0.466
HGDP-CEPH-db Supplement 1	Central_South_Asia	Sub	414	T=0.324	C=0.676
HGDP-CEPH-db Supplement 1	Middle_Est	Sub	350	T=0.260	C=0.740
HGDP-CEPH-db Supplement 1	Europe	Sub	320	T=0.250	C=0.750
HGDP-CEPH-db Supplement 1	Africa	Sub	242	T=0.244	C=0.756
HGDP-CEPH-db Supplement 1	America	Sub	216	T=0.130	C=0.870
HGDP-CEPH-db Supplement 1	Oceania	Sub	70	T=0.36	C=0.64
HapMap	Global	Study-wide	1892	T=0.2748	C=0.7252
HapMap	American	Sub	770	T=0.292	C=0.708
HapMap	African	Sub	692	T=0.194	C=0.806
HapMap	Asian	Sub	254	T=0.484	C=0.516
HapMap	Europe	Sub	176	T=0.216	C=0.784
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	T=0.239	C=0.761
CNV burdens in cranial meningiomas	Global	Study-wide	788	T=0.443	C=0.557
CNV burdens in cranial meningiomas	CRM	Sub	788	T=0.443	C=0.557
Northern Sweden	ACPOP	Study-wide	600	T=0.162	C=0.838
SGDP_PRJ	Global	Study-wide	500	T=0.232	C=0.768
Qatari	Global	Study-wide	216	T=0.231	C=0.769
A Vietnamese Genetic Variation Database	Global	Study-wide	216	T=0.537	C=0.463
Ancient Sardinia genome-wide 1240k capture data generation and analysis	Global	Study-wide	88	T=0.43	C=0.57
Siberian	Global	Study-wide	46	T=0.26	C=0.74
The Danish reference pan genome	Danish	Study-wide	40	T=0.38	C=0.62

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 8	NC_000008.11:g.141354063T>C
GRCh37.p13 chr 8	NC_000008.10:g.142364163T>C
GRCh38.p14 chr 8 fix patch HG2031_PATCH	NW_025791786.1:g.20617T>C
GRCh38.p14 chr 8 alt locus HSCHR8_5_CTG7	NT_187574.1:g.20617T>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

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	T=	C
GRCh38.p14 chr 8	NC_000008.11:g.141354063=	NC_000008.11:g.141354063T>C
GRCh37.p13 chr 8	NC_000008.10:g.142364163=	NC_000008.10:g.142364163T>C
GRCh38.p14 chr 8 fix patch HG2031_PATCH	NW_025791786.1:g.20617=	NW_025791786.1:g.20617T>C
GRCh38.p14 chr 8 alt locus HSCHR8_5_CTG7	NT_187574.1:g.20617=	NT_187574.1:g.20617T>C

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#.

140 SubSNP, 23 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	CSHL-HAPMAP	ss17236975	Feb 27, 2004 (120)
2	SSAHASNP	ss22697005	Apr 05, 2004 (121)
3	ILLUMINA	ss66750503	Dec 01, 2006 (127)
4	ILLUMINA	ss67405200	Dec 01, 2006 (127)
5	ILLUMINA	ss67772695	Dec 01, 2006 (127)
6	ILLUMINA	ss70839359	May 25, 2008 (130)
7	ILLUMINA	ss71423040	May 17, 2007 (127)
8	ILLUMINA	ss75737829	Dec 06, 2007 (129)
9	HGSV	ss77481848	Dec 06, 2007 (129)
10	HGSV	ss78962830	Dec 06, 2007 (129)
11	ILLUMINA	ss79204609	Dec 15, 2007 (130)
12	HGSV	ss83626052	Dec 15, 2007 (130)
13	KRIBB_YJKIM	ss84411784	Dec 15, 2007 (130)
14	BCMHGSC_JDW	ss93985278	Mar 25, 2008 (129)
15	HUMANGENOME_JCVI	ss97909880	Feb 05, 2009 (130)
16	1000GENOMES	ss108483361	Jan 23, 2009 (130)
17	1000GENOMES	ss113935916	Jan 25, 2009 (130)
18	ILLUMINA-UK	ss116245533	Feb 14, 2009 (130)
19	ILLUMINA	ss122443567	Dec 01, 2009 (131)
20	ENSEMBL	ss143323512	Dec 01, 2009 (131)
21	ENSEMBL	ss143853884	Dec 01, 2009 (131)
22	ILLUMINA	ss154332508	Dec 01, 2009 (131)
23	ILLUMINA	ss159508989	Dec 01, 2009 (131)
24	ILLUMINA	ss160732930	Dec 01, 2009 (131)
25	COMPLETE_GENOMICS	ss162894729	Jul 04, 2010 (132)
26	ILLUMINA	ss171995842	Jul 04, 2010 (132)
27	ILLUMINA	ss173892978	Jul 04, 2010 (132)
28	BUSHMAN	ss199915856	Jul 04, 2010 (132)
29	BCM-HGSC-SUB	ss206472150	Jul 04, 2010 (132)
30	1000GENOMES	ss224044138	Jul 14, 2010 (132)
31	1000GENOMES	ss234672926	Jul 15, 2010 (132)
32	1000GENOMES	ss241476783	Jul 15, 2010 (132)
33	ILLUMINA	ss244302215	Jul 04, 2010 (132)
34	BL	ss254725778	May 09, 2011 (134)
35	GMI	ss280048040	May 04, 2012 (137)
36	GMI	ss285945594	Apr 25, 2013 (138)
37	PJP	ss294205861	May 09, 2011 (134)
38	ILLUMINA	ss481116806	May 04, 2012 (137)
39	ILLUMINA	ss481138856	May 04, 2012 (137)
40	ILLUMINA	ss482128495	Sep 08, 2015 (146)
41	ILLUMINA	ss485353479	May 04, 2012 (137)
42	ILLUMINA	ss537299471	Sep 08, 2015 (146)
43	TISHKOFF	ss561143982	Apr 25, 2013 (138)
44	SSMP	ss655574779	Apr 25, 2013 (138)
45	ILLUMINA	ss778926594	Aug 21, 2014 (142)
46	ILLUMINA	ss783122457	Aug 21, 2014 (142)
47	ILLUMINA	ss784079204	Aug 21, 2014 (142)
48	ILLUMINA	ss825535127	Apr 01, 2015 (144)
49	ILLUMINA	ss832381254	Apr 01, 2015 (144)
50	ILLUMINA	ss833020312	Aug 21, 2014 (142)
51	ILLUMINA	ss833611140	Aug 21, 2014 (142)
52	ILLUMINA	ss834388079	Aug 21, 2014 (142)
53	EVA-GONL	ss986170440	Aug 21, 2014 (142)
54	JMKIDD_LAB	ss1076004646	Aug 21, 2014 (142)
55	1000GENOMES	ss1332343003	Aug 21, 2014 (142)
56	DDI	ss1431704952	Apr 01, 2015 (144)
57	EVA_GENOME_DK	ss1582931405	Apr 01, 2015 (144)
58	EVA_DECODE	ss1595792547	Apr 01, 2015 (144)
59	EVA_UK10K_ALSPAC	ss1621967703	Apr 01, 2015 (144)
60	EVA_UK10K_TWINSUK	ss1664961736	Apr 01, 2015 (144)
61	EVA_SVP	ss1713080052	Apr 01, 2015 (144)
62	ILLUMINA	ss1752717624	Sep 08, 2015 (146)
63	HAMMER_LAB	ss1805813771	Sep 08, 2015 (146)
64	WEILL_CORNELL_DGM	ss1929442668	Feb 12, 2016 (147)
65	ILLUMINA	ss1946249104	Feb 12, 2016 (147)
66	ILLUMINA	ss1959151590	Feb 12, 2016 (147)
67	GENOMED	ss1971121911	Jul 19, 2016 (147)
68	JJLAB	ss2025428415	Sep 14, 2016 (149)
69	USC_VALOUEV	ss2153657262	Dec 20, 2016 (150)
70	HUMAN_LONGEVITY	ss2308263367	Dec 20, 2016 (150)
71	SYSTEMSBIOZJU	ss2627189713	Nov 08, 2017 (151)
72	ILLUMINA	ss2634818568	Nov 08, 2017 (151)
73	ILLUMINA	ss2635190689	Nov 08, 2017 (151)
74	GRF	ss2709447752	Nov 08, 2017 (151)
75	ILLUMINA	ss2711153272	Nov 08, 2017 (151)
76	GNOMAD	ss2873878388	Nov 08, 2017 (151)
77	SWEGEN	ss3004167396	Nov 08, 2017 (151)
78	ILLUMINA	ss3022893040	Nov 08, 2017 (151)
79	BIOINF_KMB_FNS_UNIBA	ss3026502301	Nov 08, 2017 (151)
80	CSHL	ss3348457229	Nov 08, 2017 (151)
81	ILLUMINA	ss3625973696	Oct 12, 2018 (152)
82	ILLUMINA	ss3630182923	Oct 12, 2018 (152)
83	ILLUMINA	ss3632713909	Oct 12, 2018 (152)
84	ILLUMINA	ss3633519969	Oct 12, 2018 (152)
85	ILLUMINA	ss3634247509	Oct 12, 2018 (152)
86	ILLUMINA	ss3635195318	Oct 12, 2018 (152)
87	ILLUMINA	ss3635925842	Oct 12, 2018 (152)
88	ILLUMINA	ss3636938981	Oct 12, 2018 (152)
89	ILLUMINA	ss3637679101	Oct 12, 2018 (152)
90	ILLUMINA	ss3638792323	Oct 12, 2018 (152)
91	ILLUMINA	ss3639399755	Oct 12, 2018 (152)
92	ILLUMINA	ss3639731463	Oct 12, 2018 (152)
93	ILLUMINA	ss3640902609	Oct 12, 2018 (152)
94	ILLUMINA	ss3643720952	Oct 12, 2018 (152)
95	ILLUMINA	ss3644982394	Oct 12, 2018 (152)
96	URBANLAB	ss3649041087	Oct 12, 2018 (152)
97	ILLUMINA	ss3653440996	Oct 12, 2018 (152)
98	EGCUT_WGS	ss3671900424	Jul 13, 2019 (153)
99	EVA_DECODE	ss3723213654	Jul 13, 2019 (153)
100	ILLUMINA	ss3726580953	Jul 13, 2019 (153)
101	ACPOP	ss3736193889	Jul 13, 2019 (153)
102	ILLUMINA	ss3744314151	Jul 13, 2019 (153)
103	ILLUMINA	ss3745495289	Jul 13, 2019 (153)
104	EVA	ss3768744714	Jul 13, 2019 (153)
105	PAGE_CC	ss3771476150	Jul 13, 2019 (153)
106	ILLUMINA	ss3772987467	Jul 13, 2019 (153)
107	PACBIO	ss3786310767	Jul 13, 2019 (153)
108	PACBIO	ss3791540444	Jul 13, 2019 (153)
109	PACBIO	ss3796422031	Jul 13, 2019 (153)
110	KHV_HUMAN_GENOMES	ss3811906447	Jul 13, 2019 (153)
111	EVA	ss3831469811	Apr 26, 2020 (154)
112	EVA	ss3839245627	Apr 26, 2020 (154)
113	EVA	ss3844706639	Apr 26, 2020 (154)
114	HGDP	ss3847934438	Apr 26, 2020 (154)
115	SGDP_PRJ	ss3871221310	Apr 26, 2020 (154)
116	KRGDB	ss3918834859	Apr 26, 2020 (154)
117	EVA	ss3984613845	Apr 26, 2021 (155)
118	EVA	ss3985397285	Apr 26, 2021 (155)
119	EVA	ss4017419662	Apr 26, 2021 (155)
120	VINODS	ss4027074409	Apr 26, 2021 (155)
121	TOPMED	ss4807798653	Apr 26, 2021 (155)
122	TOMMO_GENOMICS	ss5191461155	Apr 26, 2021 (155)
123	1000G_HIGH_COVERAGE	ss5279311311	Oct 17, 2022 (156)
124	EVA	ss5315372694	Oct 17, 2022 (156)
125	EVA	ss5385156180	Oct 17, 2022 (156)
126	HUGCELL_USP	ss5475656180	Oct 17, 2022 (156)
127	EVA	ss5509589684	Oct 17, 2022 (156)
128	1000G_HIGH_COVERAGE	ss5570833106	Oct 17, 2022 (156)
129	SANFORD_IMAGENETICS	ss5624709486	Oct 17, 2022 (156)
130	SANFORD_IMAGENETICS	ss5646629637	Oct 17, 2022 (156)
131	TOMMO_GENOMICS	ss5734318422	Oct 17, 2022 (156)
132	EVA	ss5799772554	Oct 17, 2022 (156)
133	YY_MCH	ss5810224096	Oct 17, 2022 (156)
134	EVA	ss5831369902	Oct 17, 2022 (156)
135	EVA	ss5847349461	Oct 17, 2022 (156)
136	EVA	ss5848193455	Oct 17, 2022 (156)
137	EVA	ss5856615485	Oct 17, 2022 (156)
138	EVA	ss5891464138	Oct 17, 2022 (156)
139	EVA	ss5975894457	Oct 17, 2022 (156)
140	EVA	ss5979881421	Oct 17, 2022 (156)
141	1000Genomes	NC_000008.10 - 142364163	Oct 12, 2018 (152)
142	1000Genomes_30x	NC_000008.11 - 141354063	Oct 17, 2022 (156)
143	The Avon Longitudinal Study of Parents and Children	NC_000008.10 - 142364163	Oct 12, 2018 (152)
144	Genetic variation in the Estonian population	NC_000008.10 - 142364163	Oct 12, 2018 (152)
145	The Danish reference pan genome	NC_000008.10 - 142364163	Apr 26, 2020 (154)
146	gnomAD - Genomes	NC_000008.11 - 141354063	Apr 26, 2021 (155)
147	Genome of the Netherlands Release 5	NC_000008.10 - 142364163	Apr 26, 2020 (154)
148	HGDP-CEPH-db Supplement 1	NC_000008.9 - 142433345	Apr 26, 2020 (154)
149	HapMap	NC_000008.11 - 141354063	Apr 26, 2020 (154)
150	KOREAN population from KRGDB	NC_000008.10 - 142364163	Apr 26, 2020 (154)
151	Northern Sweden	NC_000008.10 - 142364163	Jul 13, 2019 (153)
152	The PAGE Study	NC_000008.11 - 141354063	Jul 13, 2019 (153)
153	Ancient Sardinia genome-wide 1240k capture data generation and analysis	NC_000008.10 - 142364163	Apr 26, 2021 (155)
154	CNV burdens in cranial meningiomas	NC_000008.10 - 142364163	Apr 26, 2021 (155)
155	Qatari	NC_000008.10 - 142364163	Apr 26, 2020 (154)
156	SGDP_PRJ	NC_000008.10 - 142364163	Apr 26, 2020 (154)
157	Siberian	NC_000008.10 - 142364163	Apr 26, 2020 (154)
158	8.3KJPN	NC_000008.10 - 142364163	Apr 26, 2021 (155)
159	14KJPN	NC_000008.11 - 141354063	Oct 17, 2022 (156)
160	TopMed	NC_000008.11 - 141354063	Apr 26, 2021 (155)
161	UK 10K study - Twins	NC_000008.10 - 142364163	Oct 12, 2018 (152)
162	A Vietnamese Genetic Variation Database	NC_000008.10 - 142364163	Jul 13, 2019 (153)
163	ALFA	NC_000008.11 - 141354063	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)
rs59834843	May 25, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
612330, ss77481848, ss78962830, ss83626052, ss93985278, ss108483361, ss113935916, ss116245533, ss160732930, ss162894729, ss199915856, ss206472150, ss244302215, ss254725778, ss280048040, ss285945594, ss294205861, ss481116806, ss825535127, ss1595792547, ss1713080052, ss2635190689, ss3639399755, ss3639731463, ss3643720952, ss3847934438	NC_000008.9:142433344:T:C	NC_000008.11:141354062:T:C	(self)
44556134, 24803125, 17638672, 9096342, 11063919, 26012253, 9478754, 623212, 163284, 11484598, 23238290, 6173616, 49430462, 24803125, 5508022, ss224044138, ss234672926, ss241476783, ss481138856, ss482128495, ss485353479, ss537299471, ss561143982, ss655574779, ss778926594, ss783122457, ss784079204, ss832381254, ss833020312, ss833611140, ss834388079, ss986170440, ss1076004646, ss1332343003, ss1431704952, ss1582931405, ss1621967703, ss1664961736, ss1752717624, ss1805813771, ss1929442668, ss1946249104, ss1959151590, ss1971121911, ss2025428415, ss2153657262, ss2627189713, ss2634818568, ss2709447752, ss2711153272, ss2873878388, ss3004167396, ss3022893040, ss3348457229, ss3625973696, ss3630182923, ss3632713909, ss3633519969, ss3634247509, ss3635195318, ss3635925842, ss3636938981, ss3637679101, ss3638792323, ss3640902609, ss3644982394, ss3653440996, ss3671900424, ss3736193889, ss3744314151, ss3745495289, ss3768744714, ss3772987467, ss3786310767, ss3791540444, ss3796422031, ss3831469811, ss3839245627, ss3871221310, ss3918834859, ss3984613845, ss3985397285, ss4017419662, ss5191461155, ss5315372694, ss5385156180, ss5509589684, ss5624709486, ss5646629637, ss5799772554, ss5831369902, ss5847349461, ss5848193455, ss5975894457, ss5979881421	NC_000008.10:142364162:T:C	NC_000008.11:141354062:T:C	(self)
58359041, 314158093, 3748357, 697619, 68155526, 645176213, 8864064859, ss2308263367, ss3026502301, ss3649041087, ss3723213654, ss3726580953, ss3771476150, ss3811906447, ss3844706639, ss4807798653, ss5279311311, ss5475656180, ss5570833106, ss5734318422, ss5810224096, ss5856615485, ss5891464138	NC_000008.11:141354062:T:C	NC_000008.11:141354062:T:C	(self)
ss66750503, ss67405200, ss67772695, ss70839359, ss71423040, ss75737829, ss79204609, ss84411784, ss97909880, ss122443567, ss143323512, ss143853884, ss154332508, ss159508989, ss171995842, ss173892978	NT_008046.16:55637711:T:C	NC_000008.11:141354062:T:C	(self)
ss17236975, ss22697005	NT_028251.11:6889232:T:C	NC_000008.11:141354062:T:C	(self)
ss4027074409	NT_187574.1:20616:T:C	NC_000008.11:141354062:T: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 rs4961374

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

rs4961374