Name: rs1403637
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.

rs1403637

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr3:172440607 (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: C=0.392258 (112626/287122, ALFA)
C=0.287094 (75991/264690, TOPMED)
C=0.298622 (41819/140040, GnomAD) (+ 21 more)
C=0.20628 (16233/78694, PAGE_STUDY)
C=0.25239 (7132/28258, 14KJPN)
C=0.25364 (4251/16760, 8.3KJPN)
C=0.2108 (1350/6404, 1000G_30x)
C=0.2113 (1058/5008, 1000G)
C=0.3917 (1755/4480, Estonian)
C=0.3900 (1503/3854, ALSPAC)
C=0.4002 (1484/3708, TWINSUK)
C=0.1733 (506/2920, KOREAN)
C=0.2346 (489/2084, HGDP_Stanford)
C=0.1643 (301/1832, Korea1K)
C=0.1871 (311/1662, HapMap)
C=0.402 (401/998, GoNL)
C=0.167 (132/792, PRJEB37584)
C=0.362 (217/600, NorthernSweden)
C=0.477 (103/216, Qatari)
C=0.176 (38/216, Vietnamese)
T=0.388 (76/196, SGDP_PRJ)
T=0.37 (22/60, Ancient Sardinia)
T=0.45 (18/40, GENOME_DK)
T=0.46 (12/26, Siberian)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: None
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: 20231103111315

Population	Group	Sample Size	Ref Allele	Alt Allele	Ref HMOZ	Alt HMOZ	HTRZ	HWEP
Total	Global	292158	T=0.609085	C=0.390915	0.376618	0.158449	0.464933	32
European	Sub	263580	T=0.590785	C=0.409215	0.350755	0.169186	0.480059	4
African	Sub	8448	T=0.8851	C=0.1149	0.782434	0.012311	0.205256	0
African Others	Sub	364	T=0.956	C=0.044	0.912088	0.0	0.087912	0
African American	Sub	8084	T=0.8819	C=0.1181	0.776596	0.012865	0.210539	0
Asian	Sub	3632	T=0.8309	C=0.1691	0.686674	0.02478	0.288546	1
East Asian	Sub	2922	T=0.8203	C=0.1797	0.666667	0.02601	0.307324	2
Other Asian	Sub	710	T=0.875	C=0.125	0.769014	0.019718	0.211268	0
Latin American 1	Sub	1022	T=0.6683	C=0.3317	0.454012	0.117417	0.428571	0
Latin American 2	Sub	2952	T=0.7229	C=0.2771	0.519648	0.073848	0.406504	0
South Asian	Sub	5190	T=0.7767	C=0.2233	0.604624	0.051252	0.344123	0
Other	Sub	7334	T=0.6663	C=0.3337	0.455413	0.122716	0.421871	6

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	287122	T=0.607742	C=0.392258
Allele Frequency Aggregator	European	Sub	260486	T=0.590619	C=0.409381
Allele Frequency Aggregator	African	Sub	7306	T=0.8837	C=0.1163
Allele Frequency Aggregator	Other	Sub	6534	T=0.6621	C=0.3379
Allele Frequency Aggregator	South Asian	Sub	5190	T=0.7767	C=0.2233
Allele Frequency Aggregator	Asian	Sub	3632	T=0.8309	C=0.1691
Allele Frequency Aggregator	Latin American 2	Sub	2952	T=0.7229	C=0.2771
Allele Frequency Aggregator	Latin American 1	Sub	1022	T=0.6683	C=0.3317
TopMed	Global	Study-wide	264690	T=0.712906	C=0.287094
gnomAD - Genomes	Global	Study-wide	140040	T=0.701378	C=0.298622
gnomAD - Genomes	European	Sub	75818	T=0.60797	C=0.39203
gnomAD - Genomes	African	Sub	41998	T=0.87749	C=0.12251
gnomAD - Genomes	American	Sub	13628	T=0.69570	C=0.30430
gnomAD - Genomes	Ashkenazi Jewish	Sub	3320	T=0.5407	C=0.4593
gnomAD - Genomes	East Asian	Sub	3130	T=0.8073	C=0.1927
gnomAD - Genomes	Other	Sub	2146	T=0.6850	C=0.3150
The PAGE Study	Global	Study-wide	78694	T=0.79372	C=0.20628
The PAGE Study	AfricanAmerican	Sub	32512	T=0.87242	C=0.12758
The PAGE Study	Mexican	Sub	10810	T=0.74431	C=0.25569
The PAGE Study	Asian	Sub	8316	T=0.7557	C=0.2443
The PAGE Study	PuertoRican	Sub	7918	T=0.7089	C=0.2911
The PAGE Study	NativeHawaiian	Sub	4534	T=0.8057	C=0.1943
The PAGE Study	Cuban	Sub	4230	T=0.6305	C=0.3695
The PAGE Study	Dominican	Sub	3826	T=0.7350	C=0.2650
The PAGE Study	CentralAmerican	Sub	2450	T=0.7796	C=0.2204
The PAGE Study	SouthAmerican	Sub	1982	T=0.7649	C=0.2351
The PAGE Study	NativeAmerican	Sub	1260	T=0.7143	C=0.2857
The PAGE Study	SouthAsian	Sub	856	T=0.813	C=0.187
14KJPN	JAPANESE	Study-wide	28258	T=0.74761	C=0.25239
8.3KJPN	JAPANESE	Study-wide	16760	T=0.74636	C=0.25364
1000Genomes_30x	Global	Study-wide	6404	T=0.7892	C=0.2108
1000Genomes_30x	African	Sub	1786	T=0.9356	C=0.0644
1000Genomes_30x	Europe	Sub	1266	T=0.5687	C=0.4313
1000Genomes_30x	South Asian	Sub	1202	T=0.8295	C=0.1705
1000Genomes_30x	East Asian	Sub	1170	T=0.8111	C=0.1889
1000Genomes_30x	American	Sub	980	T=0.732	C=0.268
1000Genomes	Global	Study-wide	5008	T=0.7887	C=0.2113
1000Genomes	African	Sub	1322	T=0.9281	C=0.0719
1000Genomes	East Asian	Sub	1008	T=0.8105	C=0.1895
1000Genomes	Europe	Sub	1006	T=0.5825	C=0.4175
1000Genomes	South Asian	Sub	978	T=0.831	C=0.169
1000Genomes	American	Sub	694	T=0.731	C=0.269
Genetic variation in the Estonian population	Estonian	Study-wide	4480	T=0.6083	C=0.3917
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	T=0.6100	C=0.3900
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	T=0.5998	C=0.4002
KOREAN population from KRGDB	KOREAN	Study-wide	2920	T=0.8267	C=0.1733
HGDP-CEPH-db Supplement 1	Global	Study-wide	2084	T=0.7654	C=0.2346
HGDP-CEPH-db Supplement 1	Est_Asia	Sub	470	T=0.872	C=0.128
HGDP-CEPH-db Supplement 1	Central_South_Asia	Sub	414	T=0.713	C=0.287
HGDP-CEPH-db Supplement 1	Middle_Est	Sub	350	T=0.583	C=0.417
HGDP-CEPH-db Supplement 1	Europe	Sub	320	T=0.569	C=0.431
HGDP-CEPH-db Supplement 1	Africa	Sub	242	T=0.930	C=0.070
HGDP-CEPH-db Supplement 1	America	Sub	216	T=0.968	C=0.032
HGDP-CEPH-db Supplement 1	Oceania	Sub	72	T=0.97	C=0.03
Korean Genome Project	KOREAN	Study-wide	1832	T=0.8357	C=0.1643
HapMap	Global	Study-wide	1662	T=0.8129	C=0.1871
HapMap	African	Sub	692	T=0.863	C=0.137
HapMap	American	Sub	542	T=0.832	C=0.168
HapMap	Asian	Sub	252	T=0.774	C=0.226
HapMap	Europe	Sub	176	T=0.614	C=0.386
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	T=0.598	C=0.402
CNV burdens in cranial meningiomas	Global	Study-wide	792	T=0.833	C=0.167
CNV burdens in cranial meningiomas	CRM	Sub	792	T=0.833	C=0.167
Northern Sweden	ACPOP	Study-wide	600	T=0.638	C=0.362
Qatari	Global	Study-wide	216	T=0.523	C=0.477
A Vietnamese Genetic Variation Database	Global	Study-wide	216	T=0.824	C=0.176
SGDP_PRJ	Global	Study-wide	196	T=0.388	C=0.612
Ancient Sardinia genome-wide 1240k capture data generation and analysis	Global	Study-wide	60	T=0.37	C=0.63
The Danish reference pan genome	Danish	Study-wide	40	T=0.45	C=0.55
Siberian	Global	Study-wide	26	T=0.46	C=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 3	NC_000003.12:g.172440607T>C
GRCh37.p13 chr 3	NC_000003.11:g.172158397T>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 3	NC_000003.12:g.172440607=	NC_000003.12:g.172440607T>C
GRCh37.p13 chr 3	NC_000003.11:g.172158397=	NC_000003.11:g.172158397T>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#.

142 SubSNP, 24 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	TSC-CSHL	ss2202260	Oct 23, 2000 (88)
2	SC_JCM	ss6014903	Feb 20, 2003 (111)
3	CSHL-HAPMAP	ss16989293	Feb 27, 2004 (120)
4	SSAHASNP	ss22016593	Apr 05, 2004 (121)
5	PERLEGEN	ss24357131	Sep 20, 2004 (123)
6	ABI	ss44402631	Mar 14, 2006 (126)
7	ILLUMINA	ss66606894	Nov 30, 2006 (127)
8	ILLUMINA	ss67096470	Nov 30, 2006 (127)
9	ILLUMINA	ss67431198	Nov 30, 2006 (127)
10	CSHL-HAPMAP	ss68390477	Jan 12, 2007 (127)
11	PERLEGEN	ss68882717	May 17, 2007 (127)
12	ILLUMINA	ss70429777	May 17, 2007 (127)
13	ILLUMINA	ss70614016	May 25, 2008 (130)
14	ILLUMINA	ss71161803	May 17, 2007 (127)
15	ILLUMINA	ss75473243	Dec 07, 2007 (129)
16	HGSV	ss81279050	Dec 15, 2007 (130)
17	KRIBB_YJKIM	ss83757502	Dec 15, 2007 (130)
18	HUMANGENOME_JCVI	ss96075499	Feb 06, 2009 (130)
19	BGI	ss104013168	Dec 01, 2009 (131)
20	1000GENOMES	ss111358695	Jan 25, 2009 (130)
21	1000GENOMES	ss112695898	Jan 25, 2009 (130)
22	ILLUMINA-UK	ss117379964	Feb 14, 2009 (130)
23	ILLUMINA	ss121681040	Dec 01, 2009 (131)
24	ENSEMBL	ss133164110	Dec 01, 2009 (131)
25	ILLUMINA	ss153417090	Dec 01, 2009 (131)
26	ILLUMINA	ss159265728	Dec 01, 2009 (131)
27	ILLUMINA	ss160348238	Dec 01, 2009 (131)
28	COMPLETE_GENOMICS	ss162830135	Jul 04, 2010 (132)
29	COMPLETE_GENOMICS	ss164989468	Jul 04, 2010 (132)
30	ILLUMINA	ss170469369	Jul 04, 2010 (132)
31	ILLUMINA	ss172475667	Jul 04, 2010 (132)
32	BUSHMAN	ss203531842	Jul 04, 2010 (132)
33	BCM-HGSC-SUB	ss205992025	Jul 04, 2010 (132)
34	1000GENOMES	ss220582202	Jul 14, 2010 (132)
35	1000GENOMES	ss232145133	Jul 14, 2010 (132)
36	1000GENOMES	ss239492045	Jul 15, 2010 (132)
37	GMI	ss277458511	May 04, 2012 (137)
38	GMI	ss284795922	Apr 25, 2013 (138)
39	PJP	ss292975164	May 09, 2011 (134)
40	ILLUMINA	ss410906212	Sep 17, 2011 (135)
41	ILLUMINA	ss479959011	May 04, 2012 (137)
42	ILLUMINA	ss479967462	May 04, 2012 (137)
43	ILLUMINA	ss480610838	Sep 08, 2015 (146)
44	ILLUMINA	ss484777730	May 04, 2012 (137)
45	ILLUMINA	ss536865655	Sep 08, 2015 (146)
46	TISHKOFF	ss557119520	Apr 25, 2013 (138)
47	SSMP	ss650865095	Apr 25, 2013 (138)
48	ILLUMINA	ss778805069	Sep 08, 2015 (146)
49	ILLUMINA	ss782835554	Sep 08, 2015 (146)
50	ILLUMINA	ss783800287	Sep 08, 2015 (146)
51	ILLUMINA	ss825399051	Apr 01, 2015 (144)
52	ILLUMINA	ss832089141	Sep 08, 2015 (146)
53	ILLUMINA	ss832777926	Jul 13, 2019 (153)
54	ILLUMINA	ss834265274	Sep 08, 2015 (146)
55	EVA-GONL	ss979461287	Aug 21, 2014 (142)
56	JMKIDD_LAB	ss1071058275	Aug 21, 2014 (142)
57	1000GENOMES	ss1307294161	Aug 21, 2014 (142)
58	DDI	ss1429673725	Apr 01, 2015 (144)
59	EVA_GENOME_DK	ss1580298511	Apr 01, 2015 (144)
60	EVA_DECODE	ss1588955929	Apr 01, 2015 (144)
61	EVA_UK10K_ALSPAC	ss1608816535	Apr 01, 2015 (144)
62	EVA_UK10K_TWINSUK	ss1651810568	Apr 01, 2015 (144)
63	EVA_SVP	ss1712631975	Apr 01, 2015 (144)
64	ILLUMINA	ss1752452740	Sep 08, 2015 (146)
65	WEILL_CORNELL_DGM	ss1922681504	Feb 12, 2016 (147)
66	ILLUMINA	ss1946102483	Feb 12, 2016 (147)
67	ILLUMINA	ss1958629042	Feb 12, 2016 (147)
68	JJLAB	ss2021916122	Sep 14, 2016 (149)
69	USC_VALOUEV	ss2150013659	Dec 20, 2016 (150)
70	HUMAN_LONGEVITY	ss2258206785	Dec 20, 2016 (150)
71	SYSTEMSBIOZJU	ss2625457547	Nov 08, 2017 (151)
72	ILLUMINA	ss2634044425	Nov 08, 2017 (151)
73	GRF	ss2705434378	Nov 08, 2017 (151)
74	ILLUMINA	ss2710992588	Nov 08, 2017 (151)
75	GNOMAD	ss2802394256	Nov 08, 2017 (151)
76	SWEGEN	ss2993651347	Nov 08, 2017 (151)
77	ILLUMINA	ss3022313861	Nov 08, 2017 (151)
78	BIOINF_KMB_FNS_UNIBA	ss3024726510	Nov 08, 2017 (151)
79	CSHL	ss3345398086	Nov 08, 2017 (151)
80	ILLUMINA	ss3625831476	Oct 12, 2018 (152)
81	ILLUMINA	ss3628836832	Oct 12, 2018 (152)
82	ILLUMINA	ss3631985648	Oct 12, 2018 (152)
83	ILLUMINA	ss3633317126	Oct 12, 2018 (152)
84	ILLUMINA	ss3634035219	Oct 12, 2018 (152)
85	ILLUMINA	ss3634928399	Oct 12, 2018 (152)
86	ILLUMINA	ss3635718597	Oct 12, 2018 (152)
87	ILLUMINA	ss3636626355	Oct 12, 2018 (152)
88	ILLUMINA	ss3637471035	Oct 12, 2018 (152)
89	ILLUMINA	ss3638456614	Oct 12, 2018 (152)
90	ILLUMINA	ss3639231034	Oct 12, 2018 (152)
91	ILLUMINA	ss3639635073	Oct 12, 2018 (152)
92	ILLUMINA	ss3640635696	Oct 12, 2018 (152)
93	ILLUMINA	ss3641155003	Oct 12, 2018 (152)
94	ILLUMINA	ss3641451729	Oct 12, 2018 (152)
95	ILLUMINA	ss3643410327	Oct 12, 2018 (152)
96	ILLUMINA	ss3644835144	Oct 12, 2018 (152)
97	URBANLAB	ss3647587268	Oct 12, 2018 (152)
98	ILLUMINA	ss3652794816	Oct 12, 2018 (152)
99	EGCUT_WGS	ss3661600583	Jul 13, 2019 (153)
100	EVA_DECODE	ss3710837033	Jul 13, 2019 (153)
101	ILLUMINA	ss3726081849	Jul 13, 2019 (153)
102	ACPOP	ss3730597543	Jul 13, 2019 (153)
103	ILLUMINA	ss3744226255	Jul 13, 2019 (153)
104	ILLUMINA	ss3745228379	Jul 13, 2019 (153)
105	EVA	ss3761042211	Jul 13, 2019 (153)
106	PAGE_CC	ss3771083310	Jul 13, 2019 (153)
107	ILLUMINA	ss3772723534	Jul 13, 2019 (153)
108	PACBIO	ss3784537985	Jul 13, 2019 (153)
109	PACBIO	ss3790019557	Jul 13, 2019 (153)
110	PACBIO	ss3794894211	Jul 13, 2019 (153)
111	KHV_HUMAN_GENOMES	ss3804177441	Jul 13, 2019 (153)
112	EVA	ss3828220675	Apr 25, 2020 (154)
113	EVA	ss3837543423	Apr 25, 2020 (154)
114	EVA	ss3842975547	Apr 25, 2020 (154)
115	HGDP	ss3847732375	Apr 25, 2020 (154)
116	SGDP_PRJ	ss3857569952	Apr 25, 2020 (154)
117	KRGDB	ss3903642960	Apr 25, 2020 (154)
118	KOGIC	ss3952952954	Apr 25, 2020 (154)
119	EVA	ss3984519232	Apr 26, 2021 (155)
120	EVA	ss3985037122	Apr 26, 2021 (155)
121	EVA	ss4017119323	Apr 26, 2021 (155)
122	TOPMED	ss4593577435	Apr 26, 2021 (155)
123	TOMMO_GENOMICS	ss5162866651	Apr 26, 2021 (155)
124	EVA	ss5237337589	Apr 26, 2021 (155)
125	1000G_HIGH_COVERAGE	ss5257018363	Oct 12, 2022 (156)
126	EVA	ss5314912442	Oct 12, 2022 (156)
127	EVA	ss5345083159	Oct 12, 2022 (156)
128	HUGCELL_USP	ss5456062906	Oct 12, 2022 (156)
129	EVA	ss5507312634	Oct 12, 2022 (156)
130	1000G_HIGH_COVERAGE	ss5536986336	Oct 12, 2022 (156)
131	SANFORD_IMAGENETICS	ss5624538809	Oct 12, 2022 (156)
132	SANFORD_IMAGENETICS	ss5633758567	Oct 12, 2022 (156)
133	TOMMO_GENOMICS	ss5696111719	Oct 12, 2022 (156)
134	EVA	ss5799599710	Oct 12, 2022 (156)
135	YY_MCH	ss5804494536	Oct 12, 2022 (156)
136	EVA	ss5826863785	Oct 12, 2022 (156)
137	EVA	ss5847231113	Oct 12, 2022 (156)
138	EVA	ss5847990885	Oct 12, 2022 (156)
139	EVA	ss5853961463	Oct 12, 2022 (156)
140	EVA	ss5872142955	Oct 12, 2022 (156)
141	EVA	ss5962135488	Oct 12, 2022 (156)
142	EVA	ss5979680322	Oct 12, 2022 (156)
143	1000Genomes	NC_000003.11 - 172158397	Oct 12, 2018 (152)
144	1000Genomes_30x	NC_000003.12 - 172440607	Oct 12, 2022 (156)
145	The Avon Longitudinal Study of Parents and Children	NC_000003.11 - 172158397	Oct 12, 2018 (152)
146	Genetic variation in the Estonian population	NC_000003.11 - 172158397	Oct 12, 2018 (152)
147	The Danish reference pan genome	NC_000003.11 - 172158397	Apr 25, 2020 (154)
148	gnomAD - Genomes	NC_000003.12 - 172440607	Apr 26, 2021 (155)
149	Genome of the Netherlands Release 5	NC_000003.11 - 172158397	Apr 25, 2020 (154)
150	HGDP-CEPH-db Supplement 1	NC_000003.10 - 173641091	Apr 25, 2020 (154)
151	HapMap	NC_000003.12 - 172440607	Apr 25, 2020 (154)
152	KOREAN population from KRGDB	NC_000003.11 - 172158397	Apr 25, 2020 (154)
153	Korean Genome Project	NC_000003.12 - 172440607	Apr 25, 2020 (154)
154	Northern Sweden	NC_000003.11 - 172158397	Jul 13, 2019 (153)
155	The PAGE Study	NC_000003.12 - 172440607	Jul 13, 2019 (153)
156	Ancient Sardinia genome-wide 1240k capture data generation and analysis	NC_000003.11 - 172158397	Apr 26, 2021 (155)
157	CNV burdens in cranial meningiomas	NC_000003.11 - 172158397	Apr 26, 2021 (155)
158	Qatari	NC_000003.11 - 172158397	Apr 25, 2020 (154)
159	SGDP_PRJ	NC_000003.11 - 172158397	Apr 25, 2020 (154)
160	Siberian	NC_000003.11 - 172158397	Apr 25, 2020 (154)
161	8.3KJPN	NC_000003.11 - 172158397	Apr 26, 2021 (155)
162	14KJPN	NC_000003.12 - 172440607	Oct 12, 2022 (156)
163	TopMed	NC_000003.12 - 172440607	Apr 26, 2021 (155)
164	UK 10K study - Twins	NC_000003.11 - 172158397	Oct 12, 2018 (152)
165	A Vietnamese Genetic Variation Database	NC_000003.11 - 172158397	Jul 13, 2019 (153)
166	ALFA	NC_000003.12 - 172440607	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)
rs17523642	Oct 07, 2004 (123)
rs60309697	May 25, 2008 (130)
rs386530699	Aug 21, 2014 (142)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss81279050, ss3639231034, ss3639635073	NC_000003.9:173641098:T:C	NC_000003.12:172440606:T:C	(self)
410267, ss111358695, ss112695898, ss117379964, ss162830135, ss164989468, ss203531842, ss205992025, ss277458511, ss284795922, ss292975164, ss479959011, ss825399051, ss1588955929, ss1712631975, ss3643410327, ss3847732375	NC_000003.10:173641090:T:C	NC_000003.12:172440606:T:C	(self)
18601233, 10365068, 7338831, 6463450, 4555562, 10820354, 3882408, 263049, 68585, 4723434, 9586932, 2530013, 20835958, 10365068, 2267467, ss220582202, ss232145133, ss239492045, ss479967462, ss480610838, ss484777730, ss536865655, ss557119520, ss650865095, ss778805069, ss782835554, ss783800287, ss832089141, ss832777926, ss834265274, ss979461287, ss1071058275, ss1307294161, ss1429673725, ss1580298511, ss1608816535, ss1651810568, ss1752452740, ss1922681504, ss1946102483, ss1958629042, ss2021916122, ss2150013659, ss2625457547, ss2634044425, ss2705434378, ss2710992588, ss2802394256, ss2993651347, ss3022313861, ss3345398086, ss3625831476, ss3628836832, ss3631985648, ss3633317126, ss3634035219, ss3634928399, ss3635718597, ss3636626355, ss3637471035, ss3638456614, ss3640635696, ss3641155003, ss3641451729, ss3644835144, ss3652794816, ss3661600583, ss3730597543, ss3744226255, ss3745228379, ss3761042211, ss3772723534, ss3784537985, ss3790019557, ss3794894211, ss3828220675, ss3837543423, ss3857569952, ss3903642960, ss3984519232, ss3985037122, ss4017119323, ss5162866651, ss5237337589, ss5314912442, ss5345083159, ss5507312634, ss5624538809, ss5633758567, ss5799599710, ss5826863785, ss5847231113, ss5847990885, ss5962135488, ss5979680322	NC_000003.11:172158396:T:C	NC_000003.12:172440606:T:C	(self)
24512271, 132140553, 2510517, 9330955, 304779, 29948823, 430954990, 14477474528, ss2258206785, ss3024726510, ss3647587268, ss3710837033, ss3726081849, ss3771083310, ss3804177441, ss3842975547, ss3952952954, ss4593577435, ss5257018363, ss5456062906, ss5536986336, ss5696111719, ss5804494536, ss5853961463, ss5872142955	NC_000003.12:172440606:T:C	NC_000003.12:172440606:T:C	(self)
ss16989293, ss22016593	NT_005612.14:78653554:T:C	NC_000003.12:172440606:T:C	(self)
ss2202260, ss6014903, ss24357131, ss44402631, ss66606894, ss67096470, ss67431198, ss68390477, ss68882717, ss70429777, ss70614016, ss71161803, ss75473243, ss83757502, ss96075499, ss104013168, ss121681040, ss133164110, ss153417090, ss159265728, ss160348238, ss170469369, ss172475667, ss410906212	NT_005612.16:78653542:T:C	NC_000003.12:172440606: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 rs1403637

PMID	Title	Author	Year	Journal
20404923	Family and population-based studies of variation within the ghrelin receptor locus in relation to measures of obesity.	Gjesing AP et al.	2010	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.

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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs1403637