Name: rs7595037
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.

rs7595037

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr2:68419963 (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>T
Variation Type: SNV Single Nucleotide Variation
Frequency: C=0.424768 (138103/325126, ALFA)
C=0.410869 (108753/264690, TOPMED)
C=0.432607 (60513/139880, GnomAD) (+ 20 more)
C=0.35439 (27889/78696, PAGE_STUDY)
C=0.14477 (4091/28258, 14KJPN)
C=0.14248 (2388/16760, 8.3KJPN)
C=0.3362 (2153/6404, 1000G_30x)
C=0.3285 (1645/5008, 1000G)
C=0.4701 (2106/4480, Estonian)
C=0.4429 (1707/3854, ALSPAC)
C=0.4442 (1647/3708, TWINSUK)
C=0.2510 (523/2084, HGDP_Stanford)
C=0.3457 (654/1892, HapMap)
C=0.430 (429/998, GoNL)
C=0.090 (71/790, PRJEB37584)
C=0.488 (293/600, NorthernSweden)
C=0.169 (86/510, SGDP_PRJ)
C=0.356 (77/216, Qatari)
C=0.061 (13/214, Vietnamese)
C=0.36 (28/78, Ancient Sardinia)
C=0.26 (14/54, Siberian)
C=0.38 (15/40, GENOME_DK)
C=0.2 (2/8, KOREAN)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: None
Publications: 4 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	330162	C=0.424949	T=0.575051
European	Sub	289996	C=0.437389	T=0.562611
African	Sub	9524	C=0.4747	T=0.5253
African Others	Sub	372	C=0.513	T=0.487
African American	Sub	9152	C=0.4731	T=0.5269
Asian	Sub	3936	C=0.0945	T=0.9055
East Asian	Sub	3190	C=0.1078	T=0.8922
Other Asian	Sub	746	C=0.038	T=0.962
Latin American 1	Sub	1134	C=0.4330	T=0.5670
Latin American 2	Sub	7226	C=0.2207	T=0.7793
South Asian	Sub	5224	C=0.2835	T=0.7165
Other	Sub	13122	C=0.38112	T=0.61888

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
Allele Frequency Aggregator	Total	Global	325126	C=0.424768	T=0.575232
Allele Frequency Aggregator	European	Sub	286902	C=0.437337	T=0.562663
Allele Frequency Aggregator	Other	Sub	12322	C=0.38297	T=0.61703
Allele Frequency Aggregator	African	Sub	8382	C=0.4739	T=0.5261
Allele Frequency Aggregator	Latin American 2	Sub	7226	C=0.2207	T=0.7793
Allele Frequency Aggregator	South Asian	Sub	5224	C=0.2835	T=0.7165
Allele Frequency Aggregator	Asian	Sub	3936	C=0.0945	T=0.9055
Allele Frequency Aggregator	Latin American 1	Sub	1134	C=0.4330	T=0.5670
TopMed	Global	Study-wide	264690	C=0.410869	T=0.589131
gnomAD - Genomes	Global	Study-wide	139880	C=0.432607	T=0.567393
gnomAD - Genomes	European	Sub	75788	C=0.45134	T=0.54866
gnomAD - Genomes	African	Sub	41856	C=0.47680	T=0.52320
gnomAD - Genomes	American	Sub	13648	C=0.31103	T=0.68897
gnomAD - Genomes	Ashkenazi Jewish	Sub	3318	C=0.3059	T=0.6941
gnomAD - Genomes	East Asian	Sub	3120	C=0.0920	T=0.9080
gnomAD - Genomes	Other	Sub	2150	C=0.3735	T=0.6265
The PAGE Study	Global	Study-wide	78696	C=0.35439	T=0.64561
The PAGE Study	AfricanAmerican	Sub	32514	C=0.47410	T=0.52590
The PAGE Study	Mexican	Sub	10810	C=0.21748	T=0.78252
The PAGE Study	Asian	Sub	8318	C=0.1350	T=0.8650
The PAGE Study	PuertoRican	Sub	7914	C=0.4145	T=0.5855
The PAGE Study	NativeHawaiian	Sub	4534	C=0.1427	T=0.8573
The PAGE Study	Cuban	Sub	4230	C=0.3868	T=0.6132
The PAGE Study	Dominican	Sub	3828	C=0.4261	T=0.5739
The PAGE Study	CentralAmerican	Sub	2450	C=0.2588	T=0.7412
The PAGE Study	SouthAmerican	Sub	1982	C=0.2583	T=0.7417
The PAGE Study	NativeAmerican	Sub	1260	C=0.3460	T=0.6540
The PAGE Study	SouthAsian	Sub	856	C=0.262	T=0.738
14KJPN	JAPANESE	Study-wide	28258	C=0.14477	T=0.85523
8.3KJPN	JAPANESE	Study-wide	16760	C=0.14248	T=0.85752
1000Genomes_30x	Global	Study-wide	6404	C=0.3362	T=0.6638
1000Genomes_30x	African	Sub	1786	C=0.4877	T=0.5123
1000Genomes_30x	Europe	Sub	1266	C=0.4360	T=0.5640
1000Genomes_30x	South Asian	Sub	1202	C=0.2621	T=0.7379
1000Genomes_30x	East Asian	Sub	1170	C=0.0940	T=0.9060
1000Genomes_30x	American	Sub	980	C=0.311	T=0.689
1000Genomes	Global	Study-wide	5008	C=0.3285	T=0.6715
1000Genomes	African	Sub	1322	C=0.4871	T=0.5129
1000Genomes	East Asian	Sub	1008	C=0.0962	T=0.9038
1000Genomes	Europe	Sub	1006	C=0.4334	T=0.5666
1000Genomes	South Asian	Sub	978	C=0.261	T=0.739
1000Genomes	American	Sub	694	C=0.307	T=0.693
Genetic variation in the Estonian population	Estonian	Study-wide	4480	C=0.4701	T=0.5299
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	C=0.4429	T=0.5571
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	C=0.4442	T=0.5558
HGDP-CEPH-db Supplement 1	Global	Study-wide	2084	C=0.2510	T=0.7490
HGDP-CEPH-db Supplement 1	Est_Asia	Sub	470	C=0.104	T=0.896
HGDP-CEPH-db Supplement 1	Central_South_Asia	Sub	414	C=0.285	T=0.715
HGDP-CEPH-db Supplement 1	Middle_Est	Sub	350	C=0.320	T=0.680
HGDP-CEPH-db Supplement 1	Europe	Sub	320	C=0.425	T=0.575
HGDP-CEPH-db Supplement 1	Africa	Sub	242	C=0.384	T=0.616
HGDP-CEPH-db Supplement 1	America	Sub	216	C=0.069	T=0.931
HGDP-CEPH-db Supplement 1	Oceania	Sub	72	C=0.00	T=1.00
HapMap	Global	Study-wide	1892	C=0.3457	T=0.6543
HapMap	American	Sub	770	C=0.327	T=0.673
HapMap	African	Sub	692	C=0.447	T=0.553
HapMap	Asian	Sub	254	C=0.134	T=0.866
HapMap	Europe	Sub	176	C=0.335	T=0.665
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	C=0.430	T=0.570
CNV burdens in cranial meningiomas	Global	Study-wide	790	C=0.090	T=0.910
CNV burdens in cranial meningiomas	CRM	Sub	790	C=0.090	T=0.910
Northern Sweden	ACPOP	Study-wide	600	C=0.488	T=0.512
SGDP_PRJ	Global	Study-wide	510	C=0.169	T=0.831
Qatari	Global	Study-wide	216	C=0.356	T=0.644
A Vietnamese Genetic Variation Database	Global	Study-wide	214	C=0.061	T=0.939
Ancient Sardinia genome-wide 1240k capture data generation and analysis	Global	Study-wide	78	C=0.36	T=0.64
Siberian	Global	Study-wide	54	C=0.26	T=0.74
The Danish reference pan genome	Danish	Study-wide	40	C=0.38	T=0.62
KOREAN population from KRGDB	KOREAN	Study-wide	8	C=0.2	A=0.0, T=0.8

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 2	NC_000002.12:g.68419963C>A
GRCh38.p14 chr 2	NC_000002.12:g.68419963C>T
GRCh37.p13 chr 2	NC_000002.11:g.68647095C>A
GRCh37.p13 chr 2	NC_000002.11:g.68647095C>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	C=	A	T
GRCh38.p14 chr 2	NC_000002.12:g.68419963=	NC_000002.12:g.68419963C>A	NC_000002.12:g.68419963C>T
GRCh37.p13 chr 2	NC_000002.11:g.68647095=	NC_000002.11:g.68647095C>A	NC_000002.11:g.68647095C>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#.

145 SubSNP, 23 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	WI_SSAHASNP	ss11502689	Jul 11, 2003 (116)
2	CSHL-HAPMAP	ss16877464	Feb 27, 2004 (120)
3	CSHL-HAPMAP	ss19464432	Feb 27, 2004 (120)
4	SSAHASNP	ss21729323	Apr 05, 2004 (121)
5	ABI	ss41656746	Mar 15, 2006 (126)
6	ILLUMINA	ss66659315	Dec 03, 2006 (127)
7	ILLUMINA	ss67804046	Dec 03, 2006 (127)
8	ILLUMINA	ss67974784	Dec 03, 2006 (127)
9	CSHL-HAPMAP	ss68382632	Jan 12, 2007 (127)
10	PERLEGEN	ss68818151	May 16, 2007 (127)
11	ILLUMINA	ss70936466	May 24, 2008 (130)
12	ILLUMINA	ss71539296	May 16, 2007 (127)
13	ILLUMINA	ss75501757	Dec 06, 2007 (129)
14	ILLUMINA	ss79262299	Dec 15, 2007 (130)
15	HGSV	ss81790179	Dec 15, 2007 (130)
16	HGSV	ss82385178	Dec 15, 2007 (130)
17	KRIBB_YJKIM	ss84686741	Dec 15, 2007 (130)
18	BCMHGSC_JDW	ss91198671	Mar 24, 2008 (129)
19	BGI	ss106096993	Feb 04, 2009 (130)
20	1000GENOMES	ss109608031	Jan 24, 2009 (130)
21	1000GENOMES	ss110423645	Jan 24, 2009 (130)
22	ILLUMINA-UK	ss117746302	Feb 14, 2009 (130)
23	ILLUMINA	ss122788310	Dec 01, 2009 (131)
24	ENSEMBL	ss138461975	Dec 01, 2009 (131)
25	ILLUMINA	ss154433103	Dec 01, 2009 (131)
26	GMI	ss157185391	Dec 01, 2009 (131)
27	ILLUMINA	ss159608172	Dec 01, 2009 (131)
28	ILLUMINA	ss160892977	Dec 01, 2009 (131)
29	ENSEMBL	ss161284339	Dec 01, 2009 (131)
30	COMPLETE_GENOMICS	ss163558006	Jul 04, 2010 (132)
31	COMPLETE_GENOMICS	ss164600340	Jul 04, 2010 (132)
32	ILLUMINA	ss172313630	Jul 04, 2010 (132)
33	ILLUMINA	ss174440038	Jul 04, 2010 (132)
34	BUSHMAN	ss200579850	Jul 04, 2010 (132)
35	1000GENOMES	ss219307217	Jul 14, 2010 (132)
36	1000GENOMES	ss231214347	Jul 14, 2010 (132)
37	1000GENOMES	ss238757800	Jul 15, 2010 (132)
38	BL	ss253179845	May 09, 2011 (134)
39	GMI	ss276512222	May 04, 2012 (137)
40	PJP	ss292289380	May 09, 2011 (134)
41	ILLUMINA	ss481609326	May 04, 2012 (137)
42	ILLUMINA	ss481639443	May 04, 2012 (137)
43	ILLUMINA	ss482607782	Sep 08, 2015 (146)
44	ILLUMINA	ss485599553	May 04, 2012 (137)
45	ILLUMINA	ss537487960	Sep 08, 2015 (146)
46	TISHKOFF	ss555638210	Apr 25, 2013 (138)
47	SSMP	ss649227060	Apr 25, 2013 (138)
48	ILLUMINA	ss778607919	Sep 08, 2015 (146)
49	ILLUMINA	ss783245378	Sep 08, 2015 (146)
50	ILLUMINA	ss784199088	Sep 08, 2015 (146)
51	ILLUMINA	ss825592817	Apr 01, 2015 (144)
52	ILLUMINA	ss832506009	Sep 08, 2015 (146)
53	ILLUMINA	ss833119150	Jul 13, 2019 (153)
54	ILLUMINA	ss834065293	Sep 08, 2015 (146)
55	EVA-GONL	ss976957022	Aug 21, 2014 (142)
56	JMKIDD_LAB	ss1069206663	Aug 21, 2014 (142)
57	1000GENOMES	ss1297703158	Aug 21, 2014 (142)
58	DDI	ss1428612504	Apr 01, 2015 (144)
59	EVA_GENOME_DK	ss1578928188	Apr 01, 2015 (144)
60	EVA_DECODE	ss1586372012	Apr 01, 2015 (144)
61	EVA_UK10K_ALSPAC	ss1603766545	Apr 01, 2015 (144)
62	EVA_UK10K_TWINSUK	ss1646760578	Apr 01, 2015 (144)
63	EVA_SVP	ss1712464425	Apr 01, 2015 (144)
64	ILLUMINA	ss1752366657	Sep 08, 2015 (146)
65	HAMMER_LAB	ss1796902072	Sep 08, 2015 (146)
66	WEILL_CORNELL_DGM	ss1920183639	Feb 12, 2016 (147)
67	ILLUMINA	ss1946042897	Feb 12, 2016 (147)
68	ILLUMINA	ss1958426737	Feb 12, 2016 (147)
69	GENOMED	ss1968797772	Jul 19, 2016 (147)
70	JJLAB	ss2020626360	Sep 14, 2016 (149)
71	ILLUMINA	ss2094904979	Dec 20, 2016 (150)
72	ILLUMINA	ss2095094735	Dec 20, 2016 (150)
73	ILLUMINA	ss2095094736	Dec 20, 2016 (150)
74	USC_VALOUEV	ss2148671611	Dec 20, 2016 (150)
75	HUMAN_LONGEVITY	ss2231279883	Dec 20, 2016 (150)
76	SYSTEMSBIOZJU	ss2624823028	Nov 08, 2017 (151)
77	ILLUMINA	ss2633629031	Nov 08, 2017 (151)
78	GRF	ss2703244054	Nov 08, 2017 (151)
79	ILLUMINA	ss2710903625	Nov 08, 2017 (151)
80	GNOMAD	ss2774809646	Nov 08, 2017 (151)
81	AFFY	ss2985798575	Nov 08, 2017 (151)
82	SWEGEN	ss2989688912	Nov 08, 2017 (151)
83	ILLUMINA	ss3021981012	Nov 08, 2017 (151)
84	BIOINF_KMB_FNS_UNIBA	ss3024080387	Nov 08, 2017 (151)
85	CSHL	ss3344280261	Nov 08, 2017 (151)
86	ILLUMINA	ss3625757625	Oct 11, 2018 (152)
87	ILLUMINA	ss3628088274	Oct 11, 2018 (152)
88	ILLUMINA	ss3631595077	Oct 11, 2018 (152)
89	ILLUMINA	ss3633204375	Oct 11, 2018 (152)
90	ILLUMINA	ss3633916213	Oct 11, 2018 (152)
91	ILLUMINA	ss3634771333	Oct 11, 2018 (152)
92	ILLUMINA	ss3635602392	Oct 11, 2018 (152)
93	ILLUMINA	ss3636458422	Oct 11, 2018 (152)
94	ILLUMINA	ss3637354270	Oct 11, 2018 (152)
95	ILLUMINA	ss3638266565	Oct 11, 2018 (152)
96	ILLUMINA	ss3639138492	Oct 11, 2018 (152)
97	ILLUMINA	ss3639581284	Oct 11, 2018 (152)
98	ILLUMINA	ss3640478635	Oct 11, 2018 (152)
99	ILLUMINA	ss3643236067	Oct 11, 2018 (152)
100	ILLUMINA	ss3644745644	Oct 11, 2018 (152)
101	ILLUMINA	ss3652415979	Oct 11, 2018 (152)
102	ILLUMINA	ss3652415980	Oct 11, 2018 (152)
103	EGCUT_WGS	ss3657668281	Jul 13, 2019 (153)
104	EVA_DECODE	ss3704116364	Jul 13, 2019 (153)
105	ILLUMINA	ss3725794374	Jul 13, 2019 (153)
106	ACPOP	ss3728530534	Jul 13, 2019 (153)
107	ILLUMINA	ss3744177371	Jul 13, 2019 (153)
108	ILLUMINA	ss3744475992	Jul 13, 2019 (153)
109	ILLUMINA	ss3745071245	Jul 13, 2019 (153)
110	EVA	ss3756899111	Jul 13, 2019 (153)
111	PAGE_CC	ss3770926536	Jul 13, 2019 (153)
112	ILLUMINA	ss3772568043	Jul 13, 2019 (153)
113	PACBIO	ss3783891740	Jul 13, 2019 (153)
114	PACBIO	ss3789474032	Jul 13, 2019 (153)
115	PACBIO	ss3794346977	Jul 13, 2019 (153)
116	KHV_HUMAN_GENOMES	ss3801266465	Jul 13, 2019 (153)
117	EVA	ss3827037588	Apr 25, 2020 (154)
118	EVA	ss3836928552	Apr 25, 2020 (154)
119	EVA	ss3842344516	Apr 25, 2020 (154)
120	HGDP	ss3847621720	Apr 25, 2020 (154)
121	SGDP_PRJ	ss3852501136	Apr 25, 2020 (154)
122	KRGDB	ss3897935803	Apr 25, 2020 (154)
123	EVA	ss3984484234	Apr 26, 2021 (155)
124	EVA	ss3984900446	Apr 26, 2021 (155)
125	EVA	ss4017001931	Apr 26, 2021 (155)
126	TOPMED	ss4509849177	Apr 26, 2021 (155)
127	TOMMO_GENOMICS	ss5151882784	Apr 26, 2021 (155)
128	1000G_HIGH_COVERAGE	ss5248456393	Oct 12, 2022 (156)
129	EVA	ss5314743981	Oct 12, 2022 (156)
130	EVA	ss5329662979	Oct 12, 2022 (156)
131	HUGCELL_USP	ss5448623515	Oct 12, 2022 (156)
132	EVA	ss5506446683	Oct 12, 2022 (156)
133	1000G_HIGH_COVERAGE	ss5523888402	Oct 12, 2022 (156)
134	SANFORD_IMAGENETICS	ss5624448184	Oct 12, 2022 (156)
135	SANFORD_IMAGENETICS	ss5628962854	Oct 12, 2022 (156)
136	TOMMO_GENOMICS	ss5680655799	Oct 12, 2022 (156)
137	EVA	ss5799535507	Oct 12, 2022 (156)
138	YY_MCH	ss5802299410	Oct 12, 2022 (156)
139	EVA	ss5820251485	Oct 12, 2022 (156)
140	EVA	ss5847189874	Oct 12, 2022 (156)
141	EVA	ss5847871178	Oct 12, 2022 (156)
142	EVA	ss5852565977	Oct 12, 2022 (156)
143	EVA	ss5930826500	Oct 12, 2022 (156)
144	EVA	ss5955207863	Oct 12, 2022 (156)
145	EVA	ss5979570376	Oct 12, 2022 (156)
146	1000Genomes	NC_000002.11 - 68647095	Oct 11, 2018 (152)
147	1000Genomes_30x	NC_000002.12 - 68419963	Oct 12, 2022 (156)
148	The Avon Longitudinal Study of Parents and Children	NC_000002.11 - 68647095	Oct 11, 2018 (152)
149	Genetic variation in the Estonian population	NC_000002.11 - 68647095	Oct 11, 2018 (152)
150	The Danish reference pan genome	NC_000002.11 - 68647095	Apr 25, 2020 (154)
151	gnomAD - Genomes	NC_000002.12 - 68419963	Apr 26, 2021 (155)
152	Genome of the Netherlands Release 5	NC_000002.11 - 68647095	Apr 25, 2020 (154)
153	HGDP-CEPH-db Supplement 1	NC_000002.10 - 68500599	Apr 25, 2020 (154)
154	HapMap	NC_000002.12 - 68419963	Apr 25, 2020 (154)
155	KOREAN population from KRGDB	NC_000002.11 - 68647095	Apr 25, 2020 (154)
156	Northern Sweden	NC_000002.11 - 68647095	Jul 13, 2019 (153)
157	The PAGE Study	NC_000002.12 - 68419963	Jul 13, 2019 (153)
158	Ancient Sardinia genome-wide 1240k capture data generation and analysis	NC_000002.11 - 68647095	Apr 26, 2021 (155)
159	CNV burdens in cranial meningiomas	NC_000002.11 - 68647095	Apr 26, 2021 (155)
160	Qatari	NC_000002.11 - 68647095	Apr 25, 2020 (154)
161	SGDP_PRJ	NC_000002.11 - 68647095	Apr 25, 2020 (154)
162	Siberian	NC_000002.11 - 68647095	Apr 25, 2020 (154)
163	8.3KJPN	NC_000002.11 - 68647095	Apr 26, 2021 (155)
164	14KJPN	NC_000002.12 - 68419963	Oct 12, 2022 (156)
165	TopMed	NC_000002.12 - 68419963	Apr 26, 2021 (155)
166	UK 10K study - Twins	NC_000002.11 - 68647095	Oct 11, 2018 (152)
167	A Vietnamese Genetic Variation Database	NC_000002.11 - 68647095	Jul 13, 2019 (153)
168	ALFA	NC_000002.12 - 68419963	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)
rs58347768	May 24, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
5113197, ss3897935803	NC_000002.11:68647094:C:A	NC_000002.12:68419962:C:A	(self)
ss81790179, ss82385178, ss3639138492, ss3639581284	NC_000002.9:68558745:C:T	NC_000002.12:68419962:C:T	(self)
299612, ss91198671, ss109608031, ss110423645, ss117746302, ss163558006, ss164600340, ss200579850, ss253179845, ss276512222, ss292289380, ss481609326, ss825592817, ss1586372012, ss1712464425, ss2094904979, ss3643236067, ss3847621720	NC_000002.10:68500598:C:T	NC_000002.12:68419962:C:T	(self)
8663078, 4819965, 3406529, 5098442, 2118009, 5113197, 1815399, 126373, 33563, 2225569, 4518116, 1187965, 9852091, 4819965, 1044880, ss219307217, ss231214347, ss238757800, ss481639443, ss482607782, ss485599553, ss537487960, ss555638210, ss649227060, ss778607919, ss783245378, ss784199088, ss832506009, ss833119150, ss834065293, ss976957022, ss1069206663, ss1297703158, ss1428612504, ss1578928188, ss1603766545, ss1646760578, ss1752366657, ss1796902072, ss1920183639, ss1946042897, ss1958426737, ss1968797772, ss2020626360, ss2095094735, ss2095094736, ss2148671611, ss2624823028, ss2633629031, ss2703244054, ss2710903625, ss2774809646, ss2985798575, ss2989688912, ss3021981012, ss3344280261, ss3625757625, ss3628088274, ss3631595077, ss3633204375, ss3633916213, ss3634771333, ss3635602392, ss3636458422, ss3637354270, ss3638266565, ss3640478635, ss3644745644, ss3652415979, ss3652415980, ss3657668281, ss3728530534, ss3744177371, ss3744475992, ss3745071245, ss3756899111, ss3772568043, ss3783891740, ss3789474032, ss3794346977, ss3827037588, ss3836928552, ss3852501136, ss3897935803, ss3984484234, ss3984900446, ss4017001931, ss5151882784, ss5314743981, ss5329662979, ss5506446683, ss5624448184, ss5628962854, ss5799535507, ss5820251485, ss5847189874, ss5847871178, ss5955207863, ss5979570376	NC_000002.11:68647094:C:T	NC_000002.12:68419962:C:T	(self)
11414337, 61535276, 1821666, 148005, 14492903, 313672056, 11058357265, ss2231279883, ss3024080387, ss3704116364, ss3725794374, ss3770926536, ss3801266465, ss3842344516, ss4509849177, ss5248456393, ss5448623515, ss5523888402, ss5680655799, ss5802299410, ss5852565977, ss5930826500	NC_000002.12:68419962:C:T	NC_000002.12:68419962:C:T	(self)
ss11502689	NT_022184.12:47463026:C:T	NC_000002.12:68419962:C:T	(self)
ss16877464, ss19464432, ss21729323	NT_022184.13:47463026:C:T	NC_000002.12:68419962:C:T	(self)
ss41656746, ss66659315, ss67804046, ss67974784, ss68382632, ss68818151, ss70936466, ss71539296, ss75501757, ss79262299, ss84686741, ss106096993, ss122788310, ss138461975, ss154433103, ss157185391, ss159608172, ss160892977, ss161284339, ss172313630, ss174440038	NT_022184.15:47468981:C:T	NC_000002.12:68419962:C:T	(self)

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

4 citations for rs7595037

PMID	Title	Author	Year	Journal
22164203	Perspectives on the use of multiple sclerosis risk genes for prediction.	Jafari N et al.	2011	PloS one
22396755	Genomic regions associated with multiple sclerosis are active in B cells.	Disanto G et al.	2012	PloS one
23730204	Progress in multiple sclerosis genetics.	Goris A et al.	2012	Current genomics
27802296	A Risk Score for Predicting Multiple Sclerosis.	Dobson R et al.	2016	PloS one

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

rs7595037