Name: rs7910961
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.

rs7910961

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr10:6035833 (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=0.334223 (101537/303800, ALFA)
T=0.291673 (77203/264690, TOPMED)
T=0.288766 (40455/140096, GnomAD) (+ 20 more)
T=0.25763 (20275/78698, PAGE_STUDY)
T=0.09594 (2711/28258, 14KJPN)
T=0.09606 (1610/16760, 8.3KJPN)
T=0.2305 (1476/6404, 1000G_30x)
T=0.2272 (1138/5008, 1000G)
T=0.3257 (1459/4480, Estonian)
T=0.3482 (1342/3854, ALSPAC)
T=0.3166 (1174/3708, TWINSUK)
T=0.0727 (213/2930, KOREAN)
T=0.2241 (424/1892, HapMap)
T=0.0786 (144/1832, Korea1K)
T=0.2385 (270/1132, Daghestan)
T=0.333 (332/998, GoNL)
T=0.075 (59/790, PRJEB37584)
T=0.257 (154/600, NorthernSweden)
T=0.152 (77/508, SGDP_PRJ)
T=0.333 (72/216, Qatari)
T=0.056 (12/216, Vietnamese)
T=0.19 (10/54, Siberian)
T=0.40 (16/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: IL2RA : Intron Variant
LOC107984201 : Non Coding Transcript Variant
Publications: 1 citation
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	308836	T=0.333685	C=0.666315
European	Sub	269284	T=0.344937	C=0.655063
African	Sub	12162	T=0.16930	C=0.83070
African Others	Sub	456	T=0.151	C=0.849
African American	Sub	11706	T=0.17000	C=0.83000
Asian	Sub	3942	T=0.0680	C=0.9320
East Asian	Sub	3196	T=0.0707	C=0.9293
Other Asian	Sub	746	T=0.056	C=0.944
Latin American 1	Sub	1132	T=0.3198	C=0.6802
Latin American 2	Sub	7220	T=0.4814	C=0.5186
South Asian	Sub	5226	T=0.1829	C=0.8171
Other	Sub	9870	T=0.3087	C=0.6913

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	303800	T=0.334223	C=0.665777
Allele Frequency Aggregator	European	Sub	266190	T=0.345009	C=0.654991
Allele Frequency Aggregator	African	Sub	11020	T=0.16887	C=0.83113
Allele Frequency Aggregator	Other	Sub	9070	T=0.3061	C=0.6939
Allele Frequency Aggregator	Latin American 2	Sub	7220	T=0.4814	C=0.5186
Allele Frequency Aggregator	South Asian	Sub	5226	T=0.1829	C=0.8171
Allele Frequency Aggregator	Asian	Sub	3942	T=0.0680	C=0.9320
Allele Frequency Aggregator	Latin American 1	Sub	1132	T=0.3198	C=0.6802
TopMed	Global	Study-wide	264690	T=0.291673	C=0.708327
gnomAD - Genomes	Global	Study-wide	140096	T=0.288766	C=0.711234
gnomAD - Genomes	European	Sub	75876	T=0.33901	C=0.66099
gnomAD - Genomes	African	Sub	41980	T=0.17351	C=0.82649
gnomAD - Genomes	American	Sub	13640	T=0.39054	C=0.60946
gnomAD - Genomes	Ashkenazi Jewish	Sub	3318	T=0.3665	C=0.6335
gnomAD - Genomes	East Asian	Sub	3128	T=0.0668	C=0.9332
gnomAD - Genomes	Other	Sub	2154	T=0.3231	C=0.6769
The PAGE Study	Global	Study-wide	78698	T=0.25763	C=0.74237
The PAGE Study	AfricanAmerican	Sub	32512	T=0.17304	C=0.82696
The PAGE Study	Mexican	Sub	10810	T=0.47854	C=0.52146
The PAGE Study	Asian	Sub	8318	T=0.0971	C=0.9029
The PAGE Study	PuertoRican	Sub	7918	T=0.3651	C=0.6349
The PAGE Study	NativeHawaiian	Sub	4534	T=0.1173	C=0.8827
The PAGE Study	Cuban	Sub	4230	T=0.3619	C=0.6381
The PAGE Study	Dominican	Sub	3828	T=0.2908	C=0.7092
The PAGE Study	CentralAmerican	Sub	2450	T=0.4408	C=0.5592
The PAGE Study	SouthAmerican	Sub	1982	T=0.4586	C=0.5414
The PAGE Study	NativeAmerican	Sub	1260	T=0.3524	C=0.6476
The PAGE Study	SouthAsian	Sub	856	T=0.196	C=0.804
14KJPN	JAPANESE	Study-wide	28258	T=0.09594	C=0.90406
8.3KJPN	JAPANESE	Study-wide	16760	T=0.09606	C=0.90394
1000Genomes_30x	Global	Study-wide	6404	T=0.2305	C=0.7695
1000Genomes_30x	African	Sub	1786	T=0.1400	C=0.8600
1000Genomes_30x	Europe	Sub	1266	T=0.3712	C=0.6288
1000Genomes_30x	South Asian	Sub	1202	T=0.1997	C=0.8003
1000Genomes_30x	East Asian	Sub	1170	T=0.0692	C=0.9308
1000Genomes_30x	American	Sub	980	T=0.444	C=0.556
1000Genomes	Global	Study-wide	5008	T=0.2272	C=0.7728
1000Genomes	African	Sub	1322	T=0.1422	C=0.8578
1000Genomes	East Asian	Sub	1008	T=0.0685	C=0.9315
1000Genomes	Europe	Sub	1006	T=0.3688	C=0.6312
1000Genomes	South Asian	Sub	978	T=0.200	C=0.800
1000Genomes	American	Sub	694	T=0.452	C=0.548
Genetic variation in the Estonian population	Estonian	Study-wide	4480	T=0.3257	C=0.6743
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	T=0.3482	C=0.6518
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	T=0.3166	C=0.6834
KOREAN population from KRGDB	KOREAN	Study-wide	2930	T=0.0727	C=0.9273
HapMap	Global	Study-wide	1892	T=0.2241	C=0.7759
HapMap	American	Sub	770	T=0.277	C=0.723
HapMap	African	Sub	692	T=0.184	C=0.816
HapMap	Asian	Sub	254	T=0.079	C=0.921
HapMap	Europe	Sub	176	T=0.364	C=0.636
Korean Genome Project	KOREAN	Study-wide	1832	T=0.0786	C=0.9214
Genome-wide autozygosity in Daghestan	Global	Study-wide	1132	T=0.2385	C=0.7615
Genome-wide autozygosity in Daghestan	Daghestan	Sub	628	T=0.232	C=0.768
Genome-wide autozygosity in Daghestan	Near_East	Sub	140	T=0.271	C=0.729
Genome-wide autozygosity in Daghestan	Central Asia	Sub	122	T=0.213	C=0.787
Genome-wide autozygosity in Daghestan	Europe	Sub	108	T=0.296	C=0.704
Genome-wide autozygosity in Daghestan	South Asian	Sub	98	T=0.15	C=0.85
Genome-wide autozygosity in Daghestan	Caucasus	Sub	36	T=0.36	C=0.64
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	T=0.333	C=0.667
CNV burdens in cranial meningiomas	Global	Study-wide	790	T=0.075	C=0.925
CNV burdens in cranial meningiomas	CRM	Sub	790	T=0.075	C=0.925
Northern Sweden	ACPOP	Study-wide	600	T=0.257	C=0.743
SGDP_PRJ	Global	Study-wide	508	T=0.152	C=0.848
Qatari	Global	Study-wide	216	T=0.333	C=0.667
A Vietnamese Genetic Variation Database	Global	Study-wide	216	T=0.056	C=0.944
Siberian	Global	Study-wide	54	T=0.19	C=0.81
The Danish reference pan genome	Danish	Study-wide	40	T=0.40	C=0.60

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.6035833T>C
GRCh37.p13 chr 10	NC_000010.10:g.6077796T>C
IL2RA RefSeqGene (LRG_73)	NG_007403.1:g.31477A>G

Gene: IL2RA, interleukin 2 receptor subunit alpha (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
IL2RA transcript variant 1	NM_000417.3:c.65-9808A>G	N/A	Intron Variant
IL2RA transcript variant 2	NM_001308242.2:c.65-9808A… NM_001308242.2:c.65-9808A>G	N/A	Intron Variant
IL2RA transcript variant 3	NM_001308243.2:c.65-9808A… NM_001308243.2:c.65-9808A>G	N/A	Intron Variant

Gene: LOC107984201, uncharacterized LOC107984201 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
LOC107984201 transcript	XR_001747349.2:n.424T>C	N/A	Non Coding Transcript 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	T=	C
GRCh38.p14 chr 10	NC_000010.11:g.6035833=	NC_000010.11:g.6035833T>C
GRCh37.p13 chr 10	NC_000010.10:g.6077796=	NC_000010.10:g.6077796T>C
IL2RA RefSeqGene (LRG_73)	NG_007403.1:g.31477=	NG_007403.1:g.31477A>G
LOC107984201 transcript	XR_001747349.2:n.424=	XR_001747349.2:n.424T>C
LOC107984201 transcript	XR_001747349.1:n.2526=	XR_001747349.1:n.2526T>C
IL2RA transcript variant 1	NM_000417.2:c.65-9808=	NM_000417.2:c.65-9808A>G
IL2RA transcript variant 1	NM_000417.3:c.65-9808=	NM_000417.3:c.65-9808A>G
IL2RA transcript variant 2	NM_001308242.2:c.65-9808=	NM_001308242.2:c.65-9808A>G
IL2RA transcript variant 3	NM_001308243.2:c.65-9808=	NM_001308243.2:c.65-9808A>G
IL2RA transcript variant X1	XM_005252446.1:c.65-9808=	XM_005252446.1:c.65-9808A>G
IL2RA transcript variant X2	XM_005252447.1:c.65-9808=	XM_005252447.1:c.65-9808A>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#.

137 SubSNP, 23 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	WI_SSAHASNP	ss12092707	Jul 11, 2003 (116)
2	SC_SNP	ss15597645	Feb 27, 2004 (120)
3	CSHL-HAPMAP	ss19182570	Feb 27, 2004 (120)
4	PGA-UW-FHCRC	ss20422910	Apr 05, 2004 (121)
5	ABI	ss38609772	Mar 13, 2006 (126)
6	RIKENSNPRC	ss49848204	Mar 13, 2006 (126)
7	PGA-UW-FHCRC	ss52087552	Oct 15, 2006 (127)
8	JDRF_WT_DIL	ss52579835	Oct 15, 2006 (127)
9	ILLUMINA	ss75139422	Dec 06, 2007 (129)
10	HGSV	ss81053276	Dec 15, 2007 (130)
11	HGSV	ss84126676	Dec 15, 2007 (130)
12	BCMHGSC_JDW	ss88079983	Mar 23, 2008 (129)
13	BGI	ss102850099	Dec 01, 2009 (131)
14	1000GENOMES	ss109195472	Jan 23, 2009 (130)
15	1000GENOMES	ss115302310	Jan 25, 2009 (130)
16	ILLUMINA-UK	ss119002416	Feb 15, 2009 (130)
17	KRIBB_YJKIM	ss119574789	Dec 01, 2009 (131)
18	WTCCC	ss120253163	Dec 01, 2009 (131)
19	ENSEMBL	ss131660403	Dec 01, 2009 (131)
20	ILLUMINA	ss154455811	Dec 01, 2009 (131)
21	GMI	ss158139973	Dec 01, 2009 (131)
22	ILLUMINA	ss159630453	Dec 01, 2009 (131)
23	ILLUMINA	ss160928093	Dec 01, 2009 (131)
24	ENSEMBL	ss161351017	Dec 01, 2009 (131)
25	COMPLETE_GENOMICS	ss167737327	Jul 04, 2010 (132)
26	COMPLETE_GENOMICS	ss168972413	Jul 04, 2010 (132)
27	COMPLETE_GENOMICS	ss170364719	Jul 04, 2010 (132)
28	ILLUMINA	ss174614190	Jul 04, 2010 (132)
29	BUSHMAN	ss201094830	Jul 04, 2010 (132)
30	BCM-HGSC-SUB	ss207139371	Jul 04, 2010 (132)
31	1000GENOMES	ss224543462	Jul 14, 2010 (132)
32	WTCCC	ss230391194	Jul 04, 2010 (132)
33	1000GENOMES	ss235037107	Jul 15, 2010 (132)
34	1000GENOMES	ss241772913	Jul 15, 2010 (132)
35	ILLUMINA	ss244311435	Jul 04, 2010 (132)
36	BL	ss254023695	May 09, 2011 (134)
37	GMI	ss280463603	May 04, 2012 (137)
38	GMI	ss286122008	Apr 25, 2013 (138)
39	PJP	ss290899650	May 09, 2011 (134)
40	ILLUMINA	ss481715214	May 04, 2012 (137)
41	ILLUMINA	ss481746544	May 04, 2012 (137)
42	ILLUMINA	ss482713028	Sep 08, 2015 (146)
43	ILLUMINA	ss485652335	May 04, 2012 (137)
44	ILLUMINA	ss537529925	Sep 08, 2015 (146)
45	TISHKOFF	ss561744124	Apr 25, 2013 (138)
46	SSMP	ss656249836	Apr 25, 2013 (138)
47	ILLUMINA	ss779050154	Aug 21, 2014 (142)
48	ILLUMINA	ss783271728	Aug 21, 2014 (142)
49	ILLUMINA	ss784224923	Aug 21, 2014 (142)
50	ILLUMINA	ss832532768	Apr 01, 2015 (144)
51	ILLUMINA	ss833141341	Aug 21, 2014 (142)
52	ILLUMINA	ss833732169	Aug 21, 2014 (142)
53	ILLUMINA	ss834513111	Aug 21, 2014 (142)
54	EVA-GONL	ss987155025	Aug 21, 2014 (142)
55	JMKIDD_LAB	ss1076729970	Aug 21, 2014 (142)
56	1000GENOMES	ss1336122115	Aug 21, 2014 (142)
57	HAMMER_LAB	ss1397571414	Sep 08, 2015 (146)
58	DDI	ss1426208019	Apr 01, 2015 (144)
59	EVA_GENOME_DK	ss1574887419	Apr 01, 2015 (144)
60	EVA_DECODE	ss1596802731	Apr 01, 2015 (144)
61	EVA_UK10K_ALSPAC	ss1623907443	Apr 01, 2015 (144)
62	EVA_UK10K_TWINSUK	ss1666901476	Apr 01, 2015 (144)
63	EVA_SVP	ss1713153875	Apr 01, 2015 (144)
64	ILLUMINA	ss1751974214	Sep 08, 2015 (146)
65	HAMMER_LAB	ss1806237281	Sep 08, 2015 (146)
66	WEILL_CORNELL_DGM	ss1930475759	Feb 12, 2016 (147)
67	ILLUMINA	ss1946275059	Feb 12, 2016 (147)
68	ILLUMINA	ss1959236676	Feb 12, 2016 (147)
69	GENOMED	ss1967048889	Jul 19, 2016 (147)
70	JJLAB	ss2025960748	Sep 14, 2016 (149)
71	ILLUMINA	ss2094857853	Dec 20, 2016 (150)
72	ILLUMINA	ss2095004751	Dec 20, 2016 (150)
73	USC_VALOUEV	ss2154202764	Dec 20, 2016 (150)
74	HUMAN_LONGEVITY	ss2172342535	Dec 20, 2016 (150)
75	SYSTEMSBIOZJU	ss2627449209	Nov 08, 2017 (151)
76	ILLUMINA	ss2632669362	Nov 08, 2017 (151)
77	ILLUMINA	ss2635010768	Nov 08, 2017 (151)
78	GRF	ss2698426397	Nov 08, 2017 (151)
79	ILLUMINA	ss2710701715	Nov 08, 2017 (151)
80	GNOMAD	ss2885083485	Nov 08, 2017 (151)
81	SWEGEN	ss3005871843	Nov 08, 2017 (151)
82	ILLUMINA	ss3021210548	Nov 08, 2017 (151)
83	BIOINF_KMB_FNS_UNIBA	ss3026763960	Nov 08, 2017 (151)
84	CSHL	ss3348940691	Nov 08, 2017 (151)
85	ILLUMINA	ss3625572871	Oct 12, 2018 (152)
86	ILLUMINA	ss3626377490	Oct 12, 2018 (152)
87	ILLUMINA	ss3630697301	Oct 12, 2018 (152)
88	ILLUMINA	ss3632936870	Oct 12, 2018 (152)
89	ILLUMINA	ss3633633472	Oct 12, 2018 (152)
90	ILLUMINA	ss3634388246	Oct 12, 2018 (152)
91	ILLUMINA	ss3635326311	Oct 12, 2018 (152)
92	ILLUMINA	ss3636068048	Oct 12, 2018 (152)
93	ILLUMINA	ss3637076895	Oct 12, 2018 (152)
94	ILLUMINA	ss3637831604	Oct 12, 2018 (152)
95	ILLUMINA	ss3640095594	Oct 12, 2018 (152)
96	ILLUMINA	ss3642836581	Oct 12, 2018 (152)
97	ILLUMINA	ss3644527730	Oct 12, 2018 (152)
98	ILLUMINA	ss3651557940	Oct 12, 2018 (152)
99	ILLUMINA	ss3651557941	Oct 12, 2018 (152)
100	EGCUT_WGS	ss3673399148	Jul 13, 2019 (153)
101	EVA_DECODE	ss3689201875	Jul 13, 2019 (153)
102	ILLUMINA	ss3725132091	Jul 13, 2019 (153)
103	ACPOP	ss3737024638	Jul 13, 2019 (153)
104	ILLUMINA	ss3744065474	Jul 13, 2019 (153)
105	ILLUMINA	ss3744689120	Jul 13, 2019 (153)
106	EVA	ss3747696755	Jul 13, 2019 (153)
107	PAGE_CC	ss3771539295	Jul 13, 2019 (153)
108	ILLUMINA	ss3772189834	Jul 13, 2019 (153)
109	PACBIO	ss3786569482	Jul 13, 2019 (153)
110	PACBIO	ss3791763448	Jul 13, 2019 (153)
111	PACBIO	ss3796645219	Jul 13, 2019 (153)
112	KHV_HUMAN_GENOMES	ss3813059854	Jul 13, 2019 (153)
113	EVA	ss3831945701	Apr 26, 2020 (154)
114	EVA	ss3839503625	Apr 26, 2020 (154)
115	EVA	ss3844969587	Apr 26, 2020 (154)
116	SGDP_PRJ	ss3873448777	Apr 26, 2020 (154)
117	KRGDB	ss3921383648	Apr 26, 2020 (154)
118	KOGIC	ss3967126708	Apr 26, 2020 (154)
119	EVA	ss3984629072	Apr 26, 2021 (155)
120	EVA	ss4017468280	Apr 26, 2021 (155)
121	TOPMED	ss4841181454	Apr 26, 2021 (155)
122	TOMMO_GENOMICS	ss5196086880	Apr 26, 2021 (155)
123	1000G_HIGH_COVERAGE	ss5282781996	Oct 16, 2022 (156)
124	EVA	ss5315447691	Oct 16, 2022 (156)
125	EVA	ss5391348124	Oct 16, 2022 (156)
126	HUGCELL_USP	ss5478573693	Oct 16, 2022 (156)
127	EVA	ss5509891805	Oct 16, 2022 (156)
128	1000G_HIGH_COVERAGE	ss5576106214	Oct 16, 2022 (156)
129	SANFORD_IMAGENETICS	ss5648597719	Oct 16, 2022 (156)
130	TOMMO_GENOMICS	ss5740883288	Oct 16, 2022 (156)
131	EVA	ss5799802077	Oct 16, 2022 (156)
132	YY_MCH	ss5811160326	Oct 16, 2022 (156)
133	EVA	ss5823920194	Oct 16, 2022 (156)
134	EVA	ss5847585472	Oct 16, 2022 (156)
135	EVA	ss5849419685	Oct 16, 2022 (156)
136	EVA	ss5877581645	Oct 16, 2022 (156)
137	EVA	ss5939878809	Oct 16, 2022 (156)
138	1000Genomes	NC_000010.10 - 6077796	Oct 12, 2018 (152)
139	1000Genomes_30x	NC_000010.11 - 6035833	Oct 16, 2022 (156)
140	The Avon Longitudinal Study of Parents and Children	NC_000010.10 - 6077796	Oct 12, 2018 (152)
141	Genome-wide autozygosity in Daghestan	NC_000010.9 - 6117802	Apr 26, 2020 (154)
142	Genetic variation in the Estonian population	NC_000010.10 - 6077796	Oct 12, 2018 (152)
143	The Danish reference pan genome	NC_000010.10 - 6077796	Apr 26, 2020 (154)
144	gnomAD - Genomes	NC_000010.11 - 6035833	Apr 26, 2021 (155)
145	Genome of the Netherlands Release 5	NC_000010.10 - 6077796	Apr 26, 2020 (154)
146	HapMap	NC_000010.11 - 6035833	Apr 26, 2020 (154)
147	KOREAN population from KRGDB	NC_000010.10 - 6077796	Apr 26, 2020 (154)
148	Korean Genome Project	NC_000010.11 - 6035833	Apr 26, 2020 (154)
149	Northern Sweden	NC_000010.10 - 6077796	Jul 13, 2019 (153)
150	The PAGE Study	NC_000010.11 - 6035833	Jul 13, 2019 (153)
151	CNV burdens in cranial meningiomas	NC_000010.10 - 6077796	Apr 26, 2021 (155)
152	Qatari	NC_000010.10 - 6077796	Apr 26, 2020 (154)
153	SGDP_PRJ	NC_000010.10 - 6077796	Apr 26, 2020 (154)
154	Siberian	NC_000010.10 - 6077796	Apr 26, 2020 (154)
155	8.3KJPN	NC_000010.10 - 6077796	Apr 26, 2021 (155)
156	14KJPN	NC_000010.11 - 6035833	Oct 16, 2022 (156)
157	TopMed	NC_000010.11 - 6035833	Apr 26, 2021 (155)
158	UK 10K study - Twins	NC_000010.10 - 6077796	Oct 12, 2018 (152)
159	A Vietnamese Genetic Variation Database	NC_000010.10 - 6077796	Jul 13, 2019 (153)
160	ALFA	NC_000010.11 - 6035833	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)
rs58884015	May 25, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss81053276, ss84126676	NC_000010.8:6117801:T:C	NC_000010.11:6035832:T:C	(self)
43023, ss88079983, ss109195472, ss115302310, ss119002416, ss160928093, ss167737327, ss168972413, ss170364719, ss201094830, ss207139371, ss244311435, ss254023695, ss280463603, ss286122008, ss290899650, ss481715214, ss1397571414, ss1596802731, ss1713153875, ss2094857853, ss2635010768, ss3642836581	NC_000010.9:6117801:T:C	NC_000010.11:6035832:T:C	(self)
48463118, 26927311, 19137396, 2013395, 12010088, 28561042, 10309503, 178527, 12517689, 25465757, 6719118, 54056187, 26927311, 5977324, ss224543462, ss235037107, ss241772913, ss481746544, ss482713028, ss485652335, ss537529925, ss561744124, ss656249836, ss779050154, ss783271728, ss784224923, ss832532768, ss833141341, ss833732169, ss834513111, ss987155025, ss1076729970, ss1336122115, ss1426208019, ss1574887419, ss1623907443, ss1666901476, ss1751974214, ss1806237281, ss1930475759, ss1946275059, ss1959236676, ss1967048889, ss2025960748, ss2095004751, ss2154202764, ss2627449209, ss2632669362, ss2698426397, ss2710701715, ss2885083485, ss3005871843, ss3021210548, ss3348940691, ss3625572871, ss3626377490, ss3630697301, ss3632936870, ss3633633472, ss3634388246, ss3635326311, ss3636068048, ss3637076895, ss3637831604, ss3640095594, ss3644527730, ss3651557940, ss3651557941, ss3673399148, ss3737024638, ss3744065474, ss3744689120, ss3747696755, ss3772189834, ss3786569482, ss3791763448, ss3796645219, ss3831945701, ss3839503625, ss3873448777, ss3921383648, ss3984629072, ss4017468280, ss5196086880, ss5315447691, ss5391348124, ss5509891805, ss5648597719, ss5799802077, ss5823920194, ss5847585472, ss5939878809	NC_000010.10:6077795:T:C	NC_000010.11:6035832:T:C	(self)
63632149, 342361135, 329619, 23504709, 760764, 74720392, 56727109, 5112286552, ss2172342535, ss3026763960, ss3689201875, ss3725132091, ss3771539295, ss3813059854, ss3844969587, ss3967126708, ss4841181454, ss5282781996, ss5478573693, ss5576106214, ss5740883288, ss5811160326, ss5849419685, ss5877581645	NC_000010.11:6035832:T:C	NC_000010.11:6035832:T:C	(self)
ss20422910, ss38609772, ss49848204, ss52087552, ss52579835, ss75139422, ss102850099, ss119574789, ss131660403, ss154455811, ss158139973, ss159630453, ss161351017, ss174614190	NT_008705.16:6017795:T:C	NC_000010.11:6035832:T:C	(self)
ss12092707, ss15597645, ss19182570, ss120253163, ss230391194	NT_077569.2:440691:T:C	NC_000010.11:6035832:T:C	(self)

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

1 citation for rs7910961

PMID	Title	Author	Year	Journal
19956101	Overview of the Rapid Response data.	Brown WM et al.	2009	Genes and immunity

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

rs7910961