Name: rs1350666
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.

rs1350666

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr4:74358873 (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 / T>G
Variation Type: SNV Single Nucleotide Variation
Frequency: T=0.273600 (90846/332040, ALFA)
T=0.344052 (91067/264690, TOPMED)
T=0.338263 (47319/139888, GnomAD) (+ 19 more)
T=0.40198 (31636/78700, PAGE_STUDY)
T=0.42919 (12128/28258, 14KJPN)
T=0.42589 (7138/16760, 8.3KJPN)
T=0.3968 (2541/6404, 1000G_30x)
T=0.4020 (2013/5008, 1000G)
T=0.2592 (1161/4480, Estonian)
T=0.2564 (988/3854, ALSPAC)
T=0.2481 (920/3708, TWINSUK)
T=0.4863 (1425/2930, KOREAN)
T=0.3743 (780/2084, HGDP_Stanford)
T=0.4175 (784/1878, HapMap)
T=0.249 (249/998, GoNL)
T=0.250 (150/600, NorthernSweden)
T=0.259 (114/440, SGDP_PRJ)
T=0.269 (58/216, Qatari)
T=0.472 (101/214, Vietnamese)
T=0.23 (11/48, Siberian)
T=0.17 (7/40, GENOME_DK)
T=0.4 (4/10, Ancient Sardinia)

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: 20230706150541

Population	Group	Sample Size	Ref Allele	Alt Allele
Total	Global	332256	T=0.273554	C=0.726446
European	Sub	285712	T=0.255688	C=0.744312
African	Sub	10654	T=0.51596	C=0.48404
African Others	Sub	392	T=0.605	C=0.395
African American	Sub	10262	T=0.51257	C=0.48743
Asian	Sub	6592	T=0.5155	C=0.4845
East Asian	Sub	4690	T=0.5055	C=0.4945
Other Asian	Sub	1902	T=0.5400	C=0.4600
Latin American 1	Sub	1102	T=0.3094	C=0.6906
Latin American 2	Sub	6982	T=0.2002	C=0.7998
South Asian	Sub	5182	T=0.4209	C=0.5791
Other	Sub	16032	T=0.31325	C=0.68675

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	332040	T=0.273600	C=0.726400
Allele Frequency Aggregator	European	Sub	285532	T=0.255737	C=0.744263
Allele Frequency Aggregator	Other	Sub	16010	T=0.31343	C=0.68657
Allele Frequency Aggregator	African	Sub	10640	T=0.51588	C=0.48412
Allele Frequency Aggregator	Latin American 2	Sub	6982	T=0.2002	C=0.7998
Allele Frequency Aggregator	Asian	Sub	6592	T=0.5155	C=0.4845
Allele Frequency Aggregator	South Asian	Sub	5182	T=0.4209	C=0.5791
Allele Frequency Aggregator	Latin American 1	Sub	1102	T=0.3094	C=0.6906
TopMed	Global	Study-wide	264690	T=0.344052	C=0.655948
gnomAD - Genomes	Global	Study-wide	139888	T=0.338263	C=0.661737
gnomAD - Genomes	European	Sub	75772	T=0.25561	C=0.74439
gnomAD - Genomes	African	Sub	41922	T=0.51436	C=0.48564
gnomAD - Genomes	American	Sub	13612	T=0.25140	C=0.74860
gnomAD - Genomes	Ashkenazi Jewish	Sub	3320	T=0.2322	C=0.7678
gnomAD - Genomes	East Asian	Sub	3114	T=0.4888	C=0.5112
gnomAD - Genomes	Other	Sub	2148	T=0.3133	C=0.6867
The PAGE Study	Global	Study-wide	78700	T=0.40198	C=0.59802
The PAGE Study	AfricanAmerican	Sub	32514	T=0.50957	C=0.49043
The PAGE Study	Mexican	Sub	10810	T=0.20426	C=0.79574
The PAGE Study	Asian	Sub	8318	T=0.4495	C=0.5505
The PAGE Study	PuertoRican	Sub	7918	T=0.3047	C=0.6953
The PAGE Study	NativeHawaiian	Sub	4534	T=0.5313	C=0.4687
The PAGE Study	Cuban	Sub	4230	T=0.2522	C=0.7478
The PAGE Study	Dominican	Sub	3828	T=0.3681	C=0.6319
The PAGE Study	CentralAmerican	Sub	2450	T=0.2694	C=0.7306
The PAGE Study	SouthAmerican	Sub	1982	T=0.2190	C=0.7810
The PAGE Study	NativeAmerican	Sub	1260	T=0.2738	C=0.7262
The PAGE Study	SouthAsian	Sub	856	T=0.449	C=0.551
14KJPN	JAPANESE	Study-wide	28258	T=0.42919	C=0.57081
8.3KJPN	JAPANESE	Study-wide	16760	T=0.42589	C=0.57411
1000Genomes_30x	Global	Study-wide	6404	T=0.3968	C=0.6032
1000Genomes_30x	African	Sub	1786	T=0.5134	C=0.4866
1000Genomes_30x	Europe	Sub	1266	T=0.2299	C=0.7701
1000Genomes_30x	South Asian	Sub	1202	T=0.4584	C=0.5416
1000Genomes_30x	East Asian	Sub	1170	T=0.4821	C=0.5179
1000Genomes_30x	American	Sub	980	T=0.222	C=0.778
1000Genomes	Global	Study-wide	5008	T=0.4020	C=0.5980
1000Genomes	African	Sub	1322	T=0.5212	C=0.4788
1000Genomes	East Asian	Sub	1008	T=0.4782	C=0.5218
1000Genomes	Europe	Sub	1006	T=0.2296	C=0.7704
1000Genomes	South Asian	Sub	978	T=0.455	C=0.545
1000Genomes	American	Sub	694	T=0.239	C=0.761
Genetic variation in the Estonian population	Estonian	Study-wide	4480	T=0.2592	C=0.7408
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	T=0.2564	C=0.7436
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	T=0.2481	C=0.7519
KOREAN population from KRGDB	KOREAN	Study-wide	2930	T=0.4863	C=0.5137, G=0.0000
HGDP-CEPH-db Supplement 1	Global	Study-wide	2084	T=0.3743	C=0.6257
HGDP-CEPH-db Supplement 1	Est_Asia	Sub	470	T=0.485	C=0.515
HGDP-CEPH-db Supplement 1	Central_South_Asia	Sub	414	T=0.447	C=0.553
HGDP-CEPH-db Supplement 1	Middle_Est	Sub	350	T=0.283	C=0.717
HGDP-CEPH-db Supplement 1	Europe	Sub	320	T=0.212	C=0.787
HGDP-CEPH-db Supplement 1	Africa	Sub	242	T=0.599	C=0.401
HGDP-CEPH-db Supplement 1	America	Sub	216	T=0.102	C=0.898
HGDP-CEPH-db Supplement 1	Oceania	Sub	72	T=0.46	C=0.54
HapMap	Global	Study-wide	1878	T=0.4175	C=0.5825
HapMap	American	Sub	762	T=0.387	C=0.613
HapMap	African	Sub	688	T=0.485	C=0.515
HapMap	Asian	Sub	252	T=0.460	C=0.540
HapMap	Europe	Sub	176	T=0.222	C=0.778
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	T=0.249	C=0.751
Northern Sweden	ACPOP	Study-wide	600	T=0.250	C=0.750
SGDP_PRJ	Global	Study-wide	440	T=0.259	C=0.741
Qatari	Global	Study-wide	216	T=0.269	C=0.731
A Vietnamese Genetic Variation Database	Global	Study-wide	214	T=0.472	C=0.528
Siberian	Global	Study-wide	48	T=0.23	C=0.77
The Danish reference pan genome	Danish	Study-wide	40	T=0.17	C=0.82
Ancient Sardinia genome-wide 1240k capture data generation and analysis	Global	Study-wide	10	T=0.4	C=0.6

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 4	NC_000004.12:g.74358873T>C
GRCh38.p14 chr 4	NC_000004.12:g.74358873T>G
GRCh37.p13 chr 4	NC_000004.11:g.75224590T>C
GRCh37.p13 chr 4	NC_000004.11:g.75224590T>G

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	G
GRCh38.p14 chr 4	NC_000004.12:g.74358873=	NC_000004.12:g.74358873T>C	NC_000004.12:g.74358873T>G
GRCh37.p13 chr 4	NC_000004.11:g.75224590=	NC_000004.11:g.75224590T>C	NC_000004.11:g.75224590T>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#.

158 SubSNP, 22 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	TSC-CSHL	ss2129883	Oct 23, 2000 (88)
2	SC_JCM	ss5963532	Feb 20, 2003 (111)
3	BCM_SSAHASNP	ss10160602	Jul 11, 2003 (116)
4	WI_SSAHASNP	ss14624675	Dec 05, 2003 (119)
5	CSHL-HAPMAP	ss20221400	Feb 27, 2004 (120)
6	SSAHASNP	ss22159813	Apr 05, 2004 (121)
7	PERLEGEN	ss23259496	Sep 20, 2004 (123)
8	ABI	ss44585926	Mar 15, 2006 (126)
9	ILLUMINA	ss67083399	Nov 29, 2006 (127)
10	ILLUMINA	ss67416373	Nov 29, 2006 (127)
11	ILLUMINA	ss68151959	Dec 12, 2006 (127)
12	PERLEGEN	ss68902105	May 16, 2007 (127)
13	ILLUMINA	ss70607409	May 25, 2008 (130)
14	ILLUMINA	ss71154407	May 16, 2007 (127)
15	ILLUMINA	ss75565617	Dec 07, 2007 (129)
16	HGSV	ss81472913	Dec 15, 2007 (130)
17	KRIBB_YJKIM	ss83732258	Dec 15, 2007 (130)
18	BCMHGSC_JDW	ss92644735	Mar 24, 2008 (129)
19	HUMANGENOME_JCVI	ss98837956	Feb 05, 2009 (130)
20	1000GENOMES	ss108049602	Jan 22, 2009 (130)
21	ILLUMINA-UK	ss117048708	Feb 14, 2009 (130)
22	ENSEMBL	ss134640030	Dec 01, 2009 (131)
23	ENSEMBL	ss139697752	Dec 01, 2009 (131)
24	ILLUMINA	ss153382707	Dec 01, 2009 (131)
25	ILLUMINA	ss159258904	Dec 01, 2009 (131)
26	ILLUMINA	ss160340042	Dec 01, 2009 (131)
27	COMPLETE_GENOMICS	ss162239234	Jul 04, 2010 (132)
28	COMPLETE_GENOMICS	ss166757028	Jul 04, 2010 (132)
29	ILLUMINA	ss172433578	Jul 04, 2010 (132)
30	BUSHMAN	ss198701000	Jul 04, 2010 (132)
31	BCM-HGSC-SUB	ss206341227	Jul 04, 2010 (132)
32	1000GENOMES	ss221002136	Jul 14, 2010 (132)
33	1000GENOMES	ss232447262	Jul 14, 2010 (132)
34	1000GENOMES	ss239729136	Jul 15, 2010 (132)
35	BL	ss253248611	May 09, 2011 (134)
36	GMI	ss277778618	May 04, 2012 (137)
37	GMI	ss284935876	Apr 25, 2013 (138)
38	PJP	ss293102374	May 09, 2011 (134)
39	ILLUMINA	ss479935103	May 04, 2012 (137)
40	ILLUMINA	ss479943216	May 04, 2012 (137)
41	ILLUMINA	ss480578488	Sep 08, 2015 (146)
42	ILLUMINA	ss484765754	May 04, 2012 (137)
43	EXOME_CHIP	ss491357045	May 04, 2012 (137)
44	ILLUMINA	ss536856671	Sep 08, 2015 (146)
45	TISHKOFF	ss557604251	Apr 25, 2013 (138)
46	SSMP	ss651413650	Apr 25, 2013 (138)
47	ILLUMINA	ss778427962	Sep 08, 2015 (146)
48	ILLUMINA	ss780681832	Sep 08, 2015 (146)
49	ILLUMINA	ss782829596	Sep 08, 2015 (146)
50	ILLUMINA	ss783355164	Sep 08, 2015 (146)
51	ILLUMINA	ss783794417	Sep 08, 2015 (146)
52	ILLUMINA	ss832083062	Sep 08, 2015 (146)
53	ILLUMINA	ss832771136	Jul 13, 2019 (153)
54	ILLUMINA	ss833883406	Sep 08, 2015 (146)
55	EVA-GONL	ss980261173	Aug 21, 2014 (142)
56	JMKIDD_LAB	ss1071648900	Aug 21, 2014 (142)
57	1000GENOMES	ss1310289511	Aug 21, 2014 (142)
58	DDI	ss1429926845	Apr 01, 2015 (144)
59	EVA_GENOME_DK	ss1580615420	Apr 01, 2015 (144)
60	EVA_DECODE	ss1589760083	Apr 01, 2015 (144)
61	EVA_UK10K_ALSPAC	ss1610365292	Apr 01, 2015 (144)
62	EVA_UK10K_TWINSUK	ss1653359325	Apr 01, 2015 (144)
63	EVA_SVP	ss1712681295	Apr 01, 2015 (144)
64	ILLUMINA	ss1752531459	Sep 08, 2015 (146)
65	ILLUMINA	ss1752531460	Sep 08, 2015 (146)
66	HAMMER_LAB	ss1801658342	Sep 08, 2015 (146)
67	ILLUMINA	ss1917781528	Feb 12, 2016 (147)
68	WEILL_CORNELL_DGM	ss1923503734	Feb 12, 2016 (147)
69	ILLUMINA	ss1946119014	Feb 12, 2016 (147)
70	ILLUMINA	ss1946119015	Feb 12, 2016 (147)
71	ILLUMINA	ss1958693632	Feb 12, 2016 (147)
72	ILLUMINA	ss1958693633	Feb 12, 2016 (147)
73	GENOMED	ss1969776356	Jul 19, 2016 (147)
74	JJLAB	ss2022337594	Sep 14, 2016 (149)
75	USC_VALOUEV	ss2150465576	Dec 20, 2016 (150)
76	HUMAN_LONGEVITY	ss2263970166	Dec 20, 2016 (150)
77	SYSTEMSBIOZJU	ss2625668676	Nov 08, 2017 (151)
78	ILLUMINA	ss2634134740	Nov 08, 2017 (151)
79	ILLUMINA	ss2634134741	Nov 08, 2017 (151)
80	ILLUMINA	ss2634134742	Nov 08, 2017 (151)
81	ILLUMINA	ss2635133273	Nov 08, 2017 (151)
82	GRF	ss2705938721	Nov 08, 2017 (151)
83	ILLUMINA	ss2711007879	Nov 08, 2017 (151)
84	GNOMAD	ss2810869426	Nov 08, 2017 (151)
85	AFFY	ss2985295055	Nov 08, 2017 (151)
86	AFFY	ss2985920149	Nov 08, 2017 (151)
87	SWEGEN	ss2994925408	Nov 08, 2017 (151)
88	ILLUMINA	ss3022384439	Nov 08, 2017 (151)
89	ILLUMINA	ss3022384440	Nov 08, 2017 (151)
90	BIOINF_KMB_FNS_UNIBA	ss3024942468	Nov 08, 2017 (151)
91	CSHL	ss3345782098	Nov 08, 2017 (151)
92	ILLUMINA	ss3625845887	Oct 12, 2018 (152)
93	ILLUMINA	ss3628991035	Oct 12, 2018 (152)
94	ILLUMINA	ss3628991036	Oct 12, 2018 (152)
95	ILLUMINA	ss3632070230	Oct 12, 2018 (152)
96	ILLUMINA	ss3633338367	Oct 12, 2018 (152)
97	ILLUMINA	ss3634057476	Oct 12, 2018 (152)
98	ILLUMINA	ss3634956716	Oct 12, 2018 (152)
99	ILLUMINA	ss3634956717	Oct 12, 2018 (152)
100	ILLUMINA	ss3635740321	Oct 12, 2018 (152)
101	ILLUMINA	ss3636660449	Oct 12, 2018 (152)
102	ILLUMINA	ss3637492843	Oct 12, 2018 (152)
103	ILLUMINA	ss3638492820	Oct 12, 2018 (152)
104	ILLUMINA	ss3639249049	Oct 12, 2018 (152)
105	ILLUMINA	ss3639923340	Oct 12, 2018 (152)
106	ILLUMINA	ss3640664012	Oct 12, 2018 (152)
107	ILLUMINA	ss3640664013	Oct 12, 2018 (152)
108	ILLUMINA	ss3643443655	Oct 12, 2018 (152)
109	ILLUMINA	ss3643969516	Oct 12, 2018 (152)
110	ILLUMINA	ss3644851799	Oct 12, 2018 (152)
111	ILLUMINA	ss3644851800	Oct 12, 2018 (152)
112	URBANLAB	ss3647763790	Oct 12, 2018 (152)
113	ILLUMINA	ss3652869593	Oct 12, 2018 (152)
114	ILLUMINA	ss3652869594	Oct 12, 2018 (152)
115	ILLUMINA	ss3654066450	Oct 12, 2018 (152)
116	EGCUT_WGS	ss3662808798	Jul 13, 2019 (153)
117	EVA_DECODE	ss3712316691	Jul 13, 2019 (153)
118	ILLUMINA	ss3726142843	Jul 13, 2019 (153)
119	ACPOP	ss3731271224	Jul 13, 2019 (153)
120	ILLUMINA	ss3744236281	Jul 13, 2019 (153)
121	ILLUMINA	ss3744525940	Jul 13, 2019 (153)
122	ILLUMINA	ss3745256990	Jul 13, 2019 (153)
123	ILLUMINA	ss3745256991	Jul 13, 2019 (153)
124	EVA	ss3761963164	Jul 13, 2019 (153)
125	PAGE_CC	ss3771132070	Jul 13, 2019 (153)
126	ILLUMINA	ss3772751593	Jul 13, 2019 (153)
127	ILLUMINA	ss3772751594	Jul 13, 2019 (153)
128	PACBIO	ss3784755859	Jul 13, 2019 (153)
129	PACBIO	ss3790208160	Jul 13, 2019 (153)
130	PACBIO	ss3795083489	Jul 13, 2019 (153)
131	KHV_HUMAN_GENOMES	ss3805104857	Jul 13, 2019 (153)
132	EVA	ss3828613114	Apr 26, 2020 (154)
133	EVA	ss3837748237	Apr 26, 2020 (154)
134	EVA	ss3843185535	Apr 26, 2020 (154)
135	HGDP	ss3847753864	Apr 26, 2020 (154)
136	SGDP_PRJ	ss3859245573	Apr 26, 2020 (154)
137	KRGDB	ss3905501053	Apr 26, 2020 (154)
138	EVA	ss3985075946	Apr 26, 2021 (155)
139	EVA	ss4017151496	Apr 26, 2021 (155)
140	TOPMED	ss4618556930	Apr 26, 2021 (155)
141	TOMMO_GENOMICS	ss5166319098	Apr 26, 2021 (155)
142	1000G_HIGH_COVERAGE	ss5259682268	Oct 13, 2022 (156)
143	EVA	ss5314966688	Oct 13, 2022 (156)
144	EVA	ss5349874433	Oct 13, 2022 (156)
145	HUGCELL_USP	ss5458388975	Oct 13, 2022 (156)
146	1000G_HIGH_COVERAGE	ss5541026091	Oct 13, 2022 (156)
147	SANFORD_IMAGENETICS	ss5624558536	Oct 13, 2022 (156)
148	SANFORD_IMAGENETICS	ss5635315269	Oct 13, 2022 (156)
149	TOMMO_GENOMICS	ss5700831646	Oct 13, 2022 (156)
150	EVA	ss5799618010	Oct 13, 2022 (156)
151	YY_MCH	ss5805206272	Oct 13, 2022 (156)
152	EVA	ss5844183963	Oct 13, 2022 (156)
153	EVA	ss5847245041	Oct 13, 2022 (156)
154	EVA	ss5848013900	Oct 13, 2022 (156)
155	EVA	ss5854283874	Oct 13, 2022 (156)
156	EVA	ss5863986108	Oct 13, 2022 (156)
157	EVA	ss5963692158	Oct 13, 2022 (156)
158	EVA	ss5979703746	Oct 13, 2022 (156)
159	1000Genomes	NC_000004.11 - 75224590	Oct 12, 2018 (152)
160	1000Genomes_30x	NC_000004.12 - 74358873	Oct 13, 2022 (156)
161	The Avon Longitudinal Study of Parents and Children	NC_000004.11 - 75224590	Oct 12, 2018 (152)
162	Genetic variation in the Estonian population	NC_000004.11 - 75224590	Oct 12, 2018 (152)
163	The Danish reference pan genome	NC_000004.11 - 75224590	Apr 26, 2020 (154)
164	gnomAD - Genomes	NC_000004.12 - 74358873	Apr 26, 2021 (155)
165	Genome of the Netherlands Release 5	NC_000004.11 - 75224590	Apr 26, 2020 (154)
166	HGDP-CEPH-db Supplement 1	NC_000004.10 - 75443454	Apr 26, 2020 (154)
167	HapMap	NC_000004.12 - 74358873	Apr 26, 2020 (154)
168	KOREAN population from KRGDB	NC_000004.11 - 75224590	Apr 26, 2020 (154)
169	Northern Sweden	NC_000004.11 - 75224590	Jul 13, 2019 (153)
170	The PAGE Study	NC_000004.12 - 74358873	Jul 13, 2019 (153)
171	Ancient Sardinia genome-wide 1240k capture data generation and analysis	NC_000004.11 - 75224590	Apr 26, 2021 (155)
172	Qatari	NC_000004.11 - 75224590	Apr 26, 2020 (154)
173	SGDP_PRJ	NC_000004.11 - 75224590	Apr 26, 2020 (154)
174	Siberian	NC_000004.11 - 75224590	Apr 26, 2020 (154)
175	8.3KJPN	NC_000004.11 - 75224590	Apr 26, 2021 (155)
176	14KJPN	NC_000004.12 - 74358873	Oct 13, 2022 (156)
177	TopMed	NC_000004.12 - 74358873	Apr 26, 2021 (155)
178	UK 10K study - Twins	NC_000004.11 - 75224590	Oct 12, 2018 (152)
179	A Vietnamese Genetic Variation Database	NC_000004.11 - 75224590	Jul 13, 2019 (153)
180	ALFA	NC_000004.12 - 74358873	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)
rs59524781	May 25, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss81472913, ss3639249049, ss3639923340, ss3643969516	NC_000004.9:75589624:T:C	NC_000004.12:74358872:T:C	(self)
431756, ss92644735, ss108049602, ss117048708, ss162239234, ss166757028, ss198701000, ss206341227, ss253248611, ss277778618, ss284935876, ss293102374, ss479935103, ss1589760083, ss1712681295, ss2635133273, ss3643443655, ss3847753864	NC_000004.10:75443453:T:C	NC_000004.12:74358872:T:C	(self)
21704734, 12065115, 8547046, 6780359, 5329211, 12678447, 4556089, 301873, 5545664, 11262553, 2981930, 24288405, 12065115, 2656951, ss221002136, ss232447262, ss239729136, ss479943216, ss480578488, ss484765754, ss491357045, ss536856671, ss557604251, ss651413650, ss778427962, ss780681832, ss782829596, ss783355164, ss783794417, ss832083062, ss832771136, ss833883406, ss980261173, ss1071648900, ss1310289511, ss1429926845, ss1580615420, ss1610365292, ss1653359325, ss1752531459, ss1752531460, ss1801658342, ss1917781528, ss1923503734, ss1946119014, ss1946119015, ss1958693632, ss1958693633, ss1969776356, ss2022337594, ss2150465576, ss2625668676, ss2634134740, ss2634134741, ss2634134742, ss2705938721, ss2711007879, ss2810869426, ss2985295055, ss2985920149, ss2994925408, ss3022384439, ss3022384440, ss3345782098, ss3625845887, ss3628991035, ss3628991036, ss3632070230, ss3633338367, ss3634057476, ss3634956716, ss3634956717, ss3635740321, ss3636660449, ss3637492843, ss3638492820, ss3640664012, ss3640664013, ss3644851799, ss3644851800, ss3652869593, ss3652869594, ss3654066450, ss3662808798, ss3731271224, ss3744236281, ss3744525940, ss3745256990, ss3745256991, ss3761963164, ss3772751593, ss3772751594, ss3784755859, ss3790208160, ss3795083489, ss3828613114, ss3837748237, ss3859245573, ss3905501053, ss3985075946, ss4017151496, ss5166319098, ss5314966688, ss5349874433, ss5624558536, ss5635315269, ss5799618010, ss5844183963, ss5847245041, ss5848013900, ss5963692158, ss5979703746	NC_000004.11:75224589:T:C	NC_000004.12:74358872:T:C	(self)
28552026, 153751980, 2638786, 353539, 34668750, 455934486, 13818038011, ss2263970166, ss3024942468, ss3647763790, ss3712316691, ss3726142843, ss3771132070, ss3805104857, ss3843185535, ss4618556930, ss5259682268, ss5458388975, ss5541026091, ss5700831646, ss5805206272, ss5854283874, ss5863986108	NC_000004.12:74358872:T:C	NC_000004.12:74358872:T:C	(self)
ss10160602, ss14624675, ss20221400, ss22159813	NT_006216.14:3731599:T:C	NC_000004.12:74358872:T:C	(self)
ss2129883, ss5963532, ss23259496, ss44585926, ss67083399, ss67416373, ss68151959, ss68902105, ss70607409, ss71154407, ss75565617, ss83732258, ss98837956, ss134640030, ss139697752, ss153382707, ss159258904, ss160340042, ss172433578	NT_022778.16:15435256:T:C	NC_000004.12:74358872:T:C	(self)
12678447, ss3905501053	NC_000004.11:75224589:T:G	NC_000004.12:74358872:T:G	(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 rs1350666

PMID	Title	Author	Year	Journal
19384554	Genome-wide association studies in ADHD.	Franke B et al.	2009	Human genetics

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
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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.
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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs1350666