Name: rs17237367
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.

rs17237367

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr15:60739770 (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: G>A
Variation Type: SNV Single Nucleotide Variation
Frequency: A=0.195489 (51744/264690, TOPMED)
A=0.210327 (43133/205076, GENOGRAPHIC)
A=0.206993 (39139/189084, ALFA) (+ 22 more)
A=0.181722 (25420/139884, GnomAD)
A=0.23370 (6604/28258, 14KJPN)
A=0.23174 (3884/16760, 8.3KJPN)
A=0.2327 (1490/6404, 1000G_30x)
A=0.2364 (1184/5008, 1000G)
A=0.1828 (819/4480, Estonian)
A=0.2008 (774/3854, ALSPAC)
A=0.2009 (745/3708, TWINSUK)
A=0.2529 (741/2930, KOREAN)
A=0.2553 (532/2084, HGDP_Stanford)
A=0.1856 (349/1880, HapMap)
A=0.2735 (501/1832, Korea1K)
A=0.2487 (282/1134, Daghestan)
A=0.183 (183/998, GoNL)
A=0.315 (197/626, Chileans)
A=0.212 (127/600, NorthernSweden)
A=0.273 (59/216, Qatari)
G=0.398 (86/216, SGDP_PRJ)
A=0.327 (70/214, Vietnamese)
A=0.098 (10/102, Ancient Sardinia)
A=0.20 (8/40, GENOME_DK)
G=0.44 (7/16, Siberian)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: RORA : Intron 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: 20231103111315

Population	Group	Sample Size	Ref Allele	Alt Allele	Ref HMOZ	Alt HMOZ	HTRZ	HWEP
Total	Global	189084	G=0.793007	A=0.206993	0.632132	0.046117	0.321751	20
European	Sub	155566	G=0.800766	A=0.199234	0.641644	0.040112	0.318244	0
African	Sub	10364	G=0.88412	A=0.11588	0.784832	0.016596	0.198572	3
African Others	Sub	360	G=0.928	A=0.072	0.861111	0.005556	0.133333	0
African American	Sub	10004	G=0.88255	A=0.11745	0.782087	0.016993	0.20092	3
Asian	Sub	750	G=0.703	A=0.297	0.488	0.082667	0.429333	0
East Asian	Sub	572	G=0.698	A=0.302	0.475524	0.08042	0.444056	0
Other Asian	Sub	178	G=0.719	A=0.281	0.52809	0.089888	0.382022	0
Latin American 1	Sub	986	G=0.805	A=0.195	0.636917	0.026369	0.336714	2
Latin American 2	Sub	9034	G=0.6414	A=0.3586	0.413327	0.130618	0.456055	0
South Asian	Sub	5054	G=0.6731	A=0.3269	0.470518	0.124258	0.405224	9
Other	Sub	7330	G=0.7767	A=0.2233	0.60955	0.056207	0.334243	3

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
TopMed	Global	Study-wide	264690	G=0.804511	A=0.195489
Genographic Project	Global	Study-wide	205076	G=0.789673	A=0.210327
Allele Frequency Aggregator	Total	Global	189084	G=0.793007	A=0.206993
Allele Frequency Aggregator	European	Sub	155566	G=0.800766	A=0.199234
Allele Frequency Aggregator	African	Sub	10364	G=0.88412	A=0.11588
Allele Frequency Aggregator	Latin American 2	Sub	9034	G=0.6414	A=0.3586
Allele Frequency Aggregator	Other	Sub	7330	G=0.7767	A=0.2233
Allele Frequency Aggregator	South Asian	Sub	5054	G=0.6731	A=0.3269
Allele Frequency Aggregator	Latin American 1	Sub	986	G=0.805	A=0.195
Allele Frequency Aggregator	Asian	Sub	750	G=0.703	A=0.297
gnomAD - Genomes	Global	Study-wide	139884	G=0.818278	A=0.181722
gnomAD - Genomes	European	Sub	75770	G=0.80399	A=0.19601
gnomAD - Genomes	African	Sub	41920	G=0.88664	A=0.11336
gnomAD - Genomes	American	Sub	13604	G=0.71009	A=0.28991
gnomAD - Genomes	Ashkenazi Jewish	Sub	3320	G=0.8425	A=0.1575
gnomAD - Genomes	East Asian	Sub	3124	G=0.7055	A=0.2945
gnomAD - Genomes	Other	Sub	2146	G=0.8001	A=0.1999
14KJPN	JAPANESE	Study-wide	28258	G=0.76630	A=0.23370
8.3KJPN	JAPANESE	Study-wide	16760	G=0.76826	A=0.23174
1000Genomes_30x	Global	Study-wide	6404	G=0.7673	A=0.2327
1000Genomes_30x	African	Sub	1786	G=0.9177	A=0.0823
1000Genomes_30x	Europe	Sub	1266	G=0.7978	A=0.2022
1000Genomes_30x	South Asian	Sub	1202	G=0.6398	A=0.3602
1000Genomes_30x	East Asian	Sub	1170	G=0.7248	A=0.2752
1000Genomes_30x	American	Sub	980	G=0.661	A=0.339
1000Genomes	Global	Study-wide	5008	G=0.7636	A=0.2364
1000Genomes	African	Sub	1322	G=0.9168	A=0.0832
1000Genomes	East Asian	Sub	1008	G=0.7163	A=0.2837
1000Genomes	Europe	Sub	1006	G=0.8072	A=0.1928
1000Genomes	South Asian	Sub	978	G=0.637	A=0.363
1000Genomes	American	Sub	694	G=0.656	A=0.344
Genetic variation in the Estonian population	Estonian	Study-wide	4480	G=0.8172	A=0.1828
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	G=0.7992	A=0.2008
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	G=0.7991	A=0.2009
KOREAN population from KRGDB	KOREAN	Study-wide	2930	G=0.7471	A=0.2529
HGDP-CEPH-db Supplement 1	Global	Study-wide	2084	G=0.7447	A=0.2553
HGDP-CEPH-db Supplement 1	Est_Asia	Sub	470	G=0.745	A=0.255
HGDP-CEPH-db Supplement 1	Central_South_Asia	Sub	414	G=0.681	A=0.319
HGDP-CEPH-db Supplement 1	Middle_Est	Sub	350	G=0.811	A=0.189
HGDP-CEPH-db Supplement 1	Europe	Sub	320	G=0.816	A=0.184
HGDP-CEPH-db Supplement 1	Africa	Sub	242	G=0.934	A=0.066
HGDP-CEPH-db Supplement 1	America	Sub	216	G=0.417	A=0.583
HGDP-CEPH-db Supplement 1	Oceania	Sub	72	G=0.82	A=0.18
HapMap	Global	Study-wide	1880	G=0.8144	A=0.1856
HapMap	American	Sub	766	G=0.735	A=0.265
HapMap	African	Sub	684	G=0.908	A=0.092
HapMap	Asian	Sub	254	G=0.787	A=0.213
HapMap	Europe	Sub	176	G=0.835	A=0.165
Korean Genome Project	KOREAN	Study-wide	1832	G=0.7265	A=0.2735
Genome-wide autozygosity in Daghestan	Global	Study-wide	1134	G=0.7513	A=0.2487
Genome-wide autozygosity in Daghestan	Daghestan	Sub	626	G=0.767	A=0.233
Genome-wide autozygosity in Daghestan	Near_East	Sub	144	G=0.764	A=0.236
Genome-wide autozygosity in Daghestan	Central Asia	Sub	122	G=0.697	A=0.303
Genome-wide autozygosity in Daghestan	Europe	Sub	108	G=0.778	A=0.222
Genome-wide autozygosity in Daghestan	South Asian	Sub	98	G=0.65	A=0.35
Genome-wide autozygosity in Daghestan	Caucasus	Sub	36	G=0.81	A=0.19
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	G=0.817	A=0.183
Chileans	Chilean	Study-wide	626	G=0.685	A=0.315
Northern Sweden	ACPOP	Study-wide	600	G=0.788	A=0.212
Qatari	Global	Study-wide	216	G=0.727	A=0.273
SGDP_PRJ	Global	Study-wide	216	G=0.398	A=0.602
A Vietnamese Genetic Variation Database	Global	Study-wide	214	G=0.673	A=0.327
Ancient Sardinia genome-wide 1240k capture data generation and analysis	Global	Study-wide	102	G=0.902	A=0.098
The Danish reference pan genome	Danish	Study-wide	40	G=0.80	A=0.20
Siberian	Global	Study-wide	16	G=0.44	A=0.56

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 15	NC_000015.10:g.60739770G>A
GRCh37.p13 chr 15	NC_000015.9:g.61031969G>A
RORA RefSeqGene	NG_029246.1:g.494534C>T

Gene: RORA, RAR related orphan receptor A (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
RORA transcript variant 1	NM_134261.3:c.167-61084C>T	N/A	Intron Variant
RORA transcript variant 3	NM_002943.4:c.	N/A	Genic Upstream Transcript Variant
RORA transcript variant 2	NM_134260.3:c.	N/A	Genic Upstream Transcript Variant
RORA transcript variant 4	NM_134262.3:c.	N/A	Genic Upstream Transcript Variant
RORA transcript variant X4	XM_047432928.1:c.-1751-61… XM_047432928.1:c.-1751-61084C>T	N/A	Intron Variant
RORA transcript variant X1	XM_011521874.2:c.	N/A	Genic Upstream Transcript Variant
RORA transcript variant X2	XM_011521875.3:c.	N/A	Genic Upstream Transcript Variant
RORA transcript variant X3	XM_011521877.4:c.	N/A	Genic Upstream Transcript Variant
RORA transcript variant X7	XM_011521879.4:c.	N/A	Genic Upstream Transcript Variant
RORA transcript variant X5	XM_047432929.1:c.	N/A	Genic Upstream Transcript Variant
RORA transcript variant X6	XM_047432930.1:c.	N/A	Genic Upstream 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	G=	A
GRCh38.p14 chr 15	NC_000015.10:g.60739770=	NC_000015.10:g.60739770G>A
GRCh37.p13 chr 15	NC_000015.9:g.61031969=	NC_000015.9:g.61031969G>A
RORA RefSeqGene	NG_029246.1:g.494534=	NG_029246.1:g.494534C>T
RORA transcript variant 1	NM_134261.2:c.167-61084=	NM_134261.2:c.167-61084C>T
RORA transcript variant 1	NM_134261.3:c.167-61084=	NM_134261.3:c.167-61084C>T
RORA transcript variant X1	XM_005254584.1:c.29-61084=	XM_005254584.1:c.29-61084C>T
RORA transcript variant X4	XM_047432928.1:c.-1751-61084=	XM_047432928.1:c.-1751-61084C>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#.

115 SubSNP, 25 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	PERLEGEN	ss24225108	Sep 20, 2004 (123)
2	ABI	ss43778617	Mar 13, 2006 (126)
3	AFFY	ss66254627	Nov 30, 2006 (127)
4	ILLUMINA	ss67181950	Nov 30, 2006 (127)
5	ILLUMINA	ss67550968	Nov 30, 2006 (127)
6	ILLUMINA	ss68178114	Dec 12, 2006 (127)
7	PERLEGEN	ss69178424	May 17, 2007 (127)
8	ILLUMINA	ss70659992	May 26, 2008 (130)
9	ILLUMINA	ss71221045	May 17, 2007 (127)
10	ILLUMINA	ss75661474	Dec 07, 2007 (129)
11	AFFY	ss76400098	Dec 07, 2007 (129)
12	HGSV	ss78669445	Dec 07, 2007 (129)
13	KRIBB_YJKIM	ss85377047	Dec 15, 2007 (130)
14	BGI	ss103244792	Dec 01, 2009 (131)
15	1000GENOMES	ss108871425	Jan 23, 2009 (130)
16	ILLUMINA-UK	ss118253135	Feb 14, 2009 (130)
17	ENSEMBL	ss136884885	Dec 01, 2009 (131)
18	ILLUMINA	ss153655519	Dec 01, 2009 (131)
19	ILLUMINA	ss159313907	Dec 01, 2009 (131)
20	ILLUMINA	ss160436154	Dec 01, 2009 (131)
21	COMPLETE_GENOMICS	ss171202305	Jul 04, 2010 (132)
22	ILLUMINA	ss172791941	Jul 04, 2010 (132)
23	AFFY	ss173476616	Jul 04, 2010 (132)
24	BUSHMAN	ss200925528	Jul 04, 2010 (132)
25	BCM-HGSC-SUB	ss207303925	Jul 04, 2010 (132)
26	1000GENOMES	ss226928275	Jul 14, 2010 (132)
27	1000GENOMES	ss236803634	Jul 15, 2010 (132)
28	1000GENOMES	ss243186504	Jul 15, 2010 (132)
29	BL	ss255036077	May 09, 2011 (134)
30	GMI	ss282283470	May 04, 2012 (137)
31	PJP	ss291734136	May 09, 2011 (134)
32	ILLUMINA	ss480217227	May 04, 2012 (137)
33	ILLUMINA	ss480227713	May 04, 2012 (137)
34	ILLUMINA	ss480960854	Sep 08, 2015 (146)
35	ILLUMINA	ss484906586	May 04, 2012 (137)
36	ILLUMINA	ss536959981	Sep 08, 2015 (146)
37	TISHKOFF	ss564521824	Apr 25, 2013 (138)
38	SSMP	ss660252707	Apr 25, 2013 (138)
39	ILLUMINA	ss780672051	Sep 08, 2015 (146)
40	ILLUMINA	ss782899607	Sep 08, 2015 (146)
41	ILLUMINA	ss783862974	Sep 08, 2015 (146)
42	ILLUMINA	ss832154381	Sep 08, 2015 (146)
43	ILLUMINA	ss832825958	Jul 13, 2019 (153)
44	ILLUMINA	ss836168129	Sep 08, 2015 (146)
45	EVA-GONL	ss991855738	Aug 21, 2014 (142)
46	JMKIDD_LAB	ss1080180571	Aug 21, 2014 (142)
47	1000GENOMES	ss1353737067	Aug 21, 2014 (142)
48	HAMMER_LAB	ss1397699124	Sep 08, 2015 (146)
49	DDI	ss1427647281	Apr 01, 2015 (144)
50	EVA_GENOME_DK	ss1577657097	Apr 01, 2015 (144)
51	EVA_UK10K_ALSPAC	ss1633143300	Apr 01, 2015 (144)
52	EVA_UK10K_TWINSUK	ss1676137333	Apr 01, 2015 (144)
53	EVA_DECODE	ss1695876769	Apr 01, 2015 (144)
54	EVA_SVP	ss1713495117	Apr 01, 2015 (144)
55	ILLUMINA	ss1752166353	Sep 08, 2015 (146)
56	HAMMER_LAB	ss1808234952	Sep 08, 2015 (146)
57	WEILL_CORNELL_DGM	ss1935263200	Feb 12, 2016 (147)
58	GENOMED	ss1968125150	Jul 19, 2016 (147)
59	JJLAB	ss2028411200	Sep 14, 2016 (149)
60	USC_VALOUEV	ss2156815834	Dec 20, 2016 (150)
61	HUMAN_LONGEVITY	ss2207346694	Dec 20, 2016 (150)
62	ILLUMINA	ss2633238333	Nov 08, 2017 (151)
63	GRF	ss2701289785	Nov 08, 2017 (151)
64	AFFY	ss2985676195	Nov 08, 2017 (151)
65	SWEGEN	ss3013392232	Nov 08, 2017 (151)
66	BIOINF_KMB_FNS_UNIBA	ss3028029832	Nov 08, 2017 (151)
67	CSHL	ss3351146833	Nov 08, 2017 (151)
68	ILLUMINA	ss3627376824	Oct 12, 2018 (152)
69	ILLUMINA	ss3631230486	Oct 12, 2018 (152)
70	ILLUMINA	ss3633099737	Oct 12, 2018 (152)
71	ILLUMINA	ss3633804434	Oct 12, 2018 (152)
72	ILLUMINA	ss3634609917	Oct 12, 2018 (152)
73	ILLUMINA	ss3635493292	Oct 12, 2018 (152)
74	ILLUMINA	ss3636299894	Oct 12, 2018 (152)
75	ILLUMINA	ss3637244579	Oct 12, 2018 (152)
76	ILLUMINA	ss3638089505	Oct 12, 2018 (152)
77	ILLUMINA	ss3639057794	Oct 12, 2018 (152)
78	ILLUMINA	ss3639838160	Oct 12, 2018 (152)
79	ILLUMINA	ss3640317238	Oct 12, 2018 (152)
80	ILLUMINA	ss3643073478	Oct 12, 2018 (152)
81	ILLUMINA	ss3643888253	Oct 12, 2018 (152)
82	URBANLAB	ss3650369531	Oct 12, 2018 (152)
83	EGCUT_WGS	ss3680537695	Jul 13, 2019 (153)
84	EVA_DECODE	ss3698024961	Jul 13, 2019 (153)
85	ACPOP	ss3740982857	Jul 13, 2019 (153)
86	ILLUMINA	ss3744910443	Jul 13, 2019 (153)
87	EVA	ss3753170137	Jul 13, 2019 (153)
88	ILLUMINA	ss3772409085	Jul 13, 2019 (153)
89	KHV_HUMAN_GENOMES	ss3818487609	Jul 13, 2019 (153)
90	EVA	ss3834269767	Apr 27, 2020 (154)
91	EVA	ss3840733670	Apr 27, 2020 (154)
92	EVA	ss3846222720	Apr 27, 2020 (154)
93	HGDP	ss3847525931	Apr 27, 2020 (154)
94	SGDP_PRJ	ss3883059703	Apr 27, 2020 (154)
95	KRGDB	ss3932242857	Apr 27, 2020 (154)
96	KOGIC	ss3976274927	Apr 27, 2020 (154)
97	EVA	ss3985720771	Apr 27, 2021 (155)
98	EVA	ss4017705342	Apr 27, 2021 (155)
99	GNOMAD	ss4289959313	Apr 27, 2021 (155)
100	TOPMED	ss4993772514	Apr 27, 2021 (155)
101	TOMMO_GENOMICS	ss5216506703	Apr 27, 2021 (155)
102	1000G_HIGH_COVERAGE	ss5298679899	Oct 16, 2022 (156)
103	GENOGRAPHIC	ss5314565003	Oct 16, 2022 (156)
104	EVA	ss5315789431	Oct 16, 2022 (156)
105	EVA	ss5419668824	Oct 16, 2022 (156)
106	HUGCELL_USP	ss5492384634	Oct 16, 2022 (156)
107	1000G_HIGH_COVERAGE	ss5600202409	Oct 16, 2022 (156)
108	SANFORD_IMAGENETICS	ss5657646957	Oct 16, 2022 (156)
109	TOMMO_GENOMICS	ss5770402994	Oct 16, 2022 (156)
110	EVA	ss5799939823	Oct 16, 2022 (156)
111	YY_MCH	ss5815394742	Oct 16, 2022 (156)
112	EVA	ss5828293866	Oct 16, 2022 (156)
113	EVA	ss5851322263	Oct 16, 2022 (156)
114	EVA	ss5876151867	Oct 16, 2022 (156)
115	EVA	ss5949053772	Oct 16, 2022 (156)
116	1000Genomes	NC_000015.9 - 61031969	Oct 12, 2018 (152)
117	1000Genomes_30x	NC_000015.10 - 60739770	Oct 16, 2022 (156)
118	The Avon Longitudinal Study of Parents and Children	NC_000015.9 - 61031969	Oct 12, 2018 (152)
119	Chileans	NC_000015.9 - 61031969	Apr 27, 2020 (154)
120	Genome-wide autozygosity in Daghestan	NC_000015.8 - 58819261	Apr 27, 2020 (154)
121	Genetic variation in the Estonian population	NC_000015.9 - 61031969	Oct 12, 2018 (152)
122	Genographic Project	NC_000015.10 - 60739770	Oct 16, 2022 (156)
123	The Danish reference pan genome	NC_000015.9 - 61031969	Apr 27, 2020 (154)
124	gnomAD - Genomes	NC_000015.10 - 60739770	Apr 27, 2021 (155)
125	Genome of the Netherlands Release 5	NC_000015.9 - 61031969	Apr 27, 2020 (154)
126	HGDP-CEPH-db Supplement 1	NC_000015.8 - 58819261	Apr 27, 2020 (154)
127	HapMap	NC_000015.10 - 60739770	Apr 27, 2020 (154)
128	KOREAN population from KRGDB	NC_000015.9 - 61031969	Apr 27, 2020 (154)
129	Korean Genome Project	NC_000015.10 - 60739770	Apr 27, 2020 (154)
130	Northern Sweden	NC_000015.9 - 61031969	Jul 13, 2019 (153)
131	Ancient Sardinia genome-wide 1240k capture data generation and analysis	NC_000015.9 - 61031969	Apr 27, 2021 (155)
132	Qatari	NC_000015.9 - 61031969	Apr 27, 2020 (154)
133	SGDP_PRJ	NC_000015.9 - 61031969	Apr 27, 2020 (154)
134	Siberian	NC_000015.9 - 61031969	Apr 27, 2020 (154)
135	8.3KJPN	NC_000015.9 - 61031969	Apr 27, 2021 (155)
136	14KJPN	NC_000015.10 - 60739770	Oct 16, 2022 (156)
137	TopMed	NC_000015.10 - 60739770	Apr 27, 2021 (155)
138	UK 10K study - Twins	NC_000015.9 - 61031969	Oct 12, 2018 (152)
139	A Vietnamese Genetic Variation Database	NC_000015.9 - 61031969	Jul 13, 2019 (153)
140	ALFA	NC_000015.10 - 60739770	Apr 27, 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)
rs60715582	May 26, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
169273, 203823, ss66254627, ss76400098, ss78669445, ss108871425, ss118253135, ss171202305, ss173476616, ss200925528, ss207303925, ss255036077, ss282283470, ss291734136, ss480217227, ss1397699124, ss1695876769, ss1713495117, ss3639057794, ss3639838160, ss3643073478, ss3643888253, ss3847525931	NC_000015.8:58819260:G:A	NC_000015.10:60739769:G:A	(self)
66818564, 37096042, 154457, 26275943, 3885223, 16562384, 39420251, 14267722, 946698, 17305130, 35076683, 9332188, 74476010, 37096042, 8253965, ss226928275, ss236803634, ss243186504, ss480227713, ss480960854, ss484906586, ss536959981, ss564521824, ss660252707, ss780672051, ss782899607, ss783862974, ss832154381, ss832825958, ss836168129, ss991855738, ss1080180571, ss1353737067, ss1427647281, ss1577657097, ss1633143300, ss1676137333, ss1752166353, ss1808234952, ss1935263200, ss1968125150, ss2028411200, ss2156815834, ss2633238333, ss2701289785, ss2985676195, ss3013392232, ss3351146833, ss3627376824, ss3631230486, ss3633099737, ss3633804434, ss3634609917, ss3635493292, ss3636299894, ss3637244579, ss3638089505, ss3640317238, ss3680537695, ss3740982857, ss3744910443, ss3753170137, ss3772409085, ss3834269767, ss3840733670, ss3883059703, ss3932242857, ss3985720771, ss4017705342, ss5216506703, ss5315789431, ss5419668824, ss5657646957, ss5799939823, ss5828293866, ss5949053772	NC_000015.9:61031968:G:A	NC_000015.10:60739769:G:A	(self)
87728344, 119954, 471051860, 1277679, 32652928, 104240098, 209318174, 10033981103, ss2207346694, ss3028029832, ss3650369531, ss3698024961, ss3818487609, ss3846222720, ss3976274927, ss4289959313, ss4993772514, ss5298679899, ss5314565003, ss5492384634, ss5600202409, ss5770402994, ss5815394742, ss5851322263, ss5876151867	NC_000015.10:60739769:G:A	NC_000015.10:60739769:G:A	(self)
ss24225108, ss43778617, ss67181950, ss67550968, ss68178114, ss69178424, ss70659992, ss71221045, ss75661474, ss85377047, ss103244792, ss136884885, ss153655519, ss159313907, ss160436154, ss172791941	NT_010194.17:31822525:G:A	NC_000015.10:60739769:G:A	(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 rs17237367

PMID	Title	Author	Year	Journal
27928975	Assessing causality in associations between cannabis use and schizophrenia risk: a two-sample Mendelian randomization study.	Gage SH et al.	2017	Psychological medicine

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

rs17237367