Name: rs35062132
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.

rs35062132

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr3:8753021 (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 / G>C
Variation Type: SNV Single Nucleotide Variation
Frequency: C=0.000086 (12/140268, GnomAD)
C=0.000179 (18/100840, ALFA)
C=0.00121 (95/78696, PAGE_STUDY) (+ 7 more)
C=0.0014 (9/6404, 1000G_30x)
C=0.0018 (9/5008, 1000G)
C=0.0058 (17/2922, KOREAN)
C=0.003 (2/790, PRJEB37584)
C=0.009 (2/216, Vietnamese)
G=0.5 (2/4, SGDP_PRJ)
C=0.5 (2/4, SGDP_PRJ)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: OXTR : Missense Variant
Publications: 2 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	100840	G=0.999812	A=0.000010, C=0.000179
European	Sub	86272	G=0.99999	A=0.00001, C=0.00000
African	Sub	3718	G=1.0000	A=0.0000, C=0.0000
African Others	Sub	166	G=1.000	A=0.000, C=0.000
African American	Sub	3552	G=1.0000	A=0.0000, C=0.0000
Asian	Sub	3272	G=0.9954	A=0.0000, C=0.0046
East Asian	Sub	2646	G=0.9955	A=0.0000, C=0.0045
Other Asian	Sub	626	G=0.995	A=0.000, C=0.005
Latin American 1	Sub	788	G=1.000	A=0.000, C=0.000
Latin American 2	Sub	946	G=0.999	A=0.000, C=0.001
South Asian	Sub	274	G=1.000	A=0.000, C=0.000
Other	Sub	5570	G=0.9996	A=0.0000, C=0.0004

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
gnomAD - Genomes	Global	Study-wide	140268	G=0.999914	C=0.000086
gnomAD - Genomes	European	Sub	75958	G=1.00000	C=0.00000
gnomAD - Genomes	African	Sub	42036	G=0.99988	C=0.00012
gnomAD - Genomes	American	Sub	13668	G=1.00000	C=0.00000
gnomAD - Genomes	Ashkenazi Jewish	Sub	3324	G=1.0000	C=0.0000
gnomAD - Genomes	East Asian	Sub	3132	G=0.9984	C=0.0016
gnomAD - Genomes	Other	Sub	2150	G=0.9991	C=0.0009
Allele Frequency Aggregator	Total	Global	100840	G=0.999812	A=0.000010, C=0.000179
Allele Frequency Aggregator	European	Sub	86272	G=0.99999	A=0.00001, C=0.00000
Allele Frequency Aggregator	Other	Sub	5570	G=0.9996	A=0.0000, C=0.0004
Allele Frequency Aggregator	African	Sub	3718	G=1.0000	A=0.0000, C=0.0000
Allele Frequency Aggregator	Asian	Sub	3272	G=0.9954	A=0.0000, C=0.0046
Allele Frequency Aggregator	Latin American 2	Sub	946	G=0.999	A=0.000, C=0.001
Allele Frequency Aggregator	Latin American 1	Sub	788	G=1.000	A=0.000, C=0.000
Allele Frequency Aggregator	South Asian	Sub	274	G=1.000	A=0.000, C=0.000
The PAGE Study	Global	Study-wide	78696	G=0.99879	C=0.00121
The PAGE Study	AfricanAmerican	Sub	32514	G=0.99982	C=0.00018
The PAGE Study	Mexican	Sub	10810	G=1.00000	C=0.00000
The PAGE Study	Asian	Sub	8316	G=0.9911	C=0.0089
The PAGE Study	PuertoRican	Sub	7916	G=1.0000	C=0.0000
The PAGE Study	NativeHawaiian	Sub	4534	G=0.9967	C=0.0033
The PAGE Study	Cuban	Sub	4230	G=1.0000	C=0.0000
The PAGE Study	Dominican	Sub	3828	G=1.0000	C=0.0000
The PAGE Study	CentralAmerican	Sub	2450	G=1.0000	C=0.0000
The PAGE Study	SouthAmerican	Sub	1982	G=1.0000	C=0.0000
The PAGE Study	NativeAmerican	Sub	1260	G=1.0000	C=0.0000
The PAGE Study	SouthAsian	Sub	856	G=1.000	C=0.000
1000Genomes_30x	Global	Study-wide	6404	G=0.9984	A=0.0002, C=0.0014
1000Genomes_30x	African	Sub	1786	G=1.0000	A=0.0000, C=0.0000
1000Genomes_30x	Europe	Sub	1266	G=1.0000	A=0.0000, C=0.0000
1000Genomes_30x	South Asian	Sub	1202	G=1.0000	A=0.0000, C=0.0000
1000Genomes_30x	East Asian	Sub	1170	G=0.9915	A=0.0009, C=0.0077
1000Genomes_30x	American	Sub	980	G=1.000	A=0.000, C=0.000
1000Genomes	Global	Study-wide	5008	G=0.9982	C=0.0018
1000Genomes	African	Sub	1322	G=1.0000	C=0.0000
1000Genomes	East Asian	Sub	1008	G=0.9911	C=0.0089
1000Genomes	Europe	Sub	1006	G=1.0000	C=0.0000
1000Genomes	South Asian	Sub	978	G=1.000	C=0.000
1000Genomes	American	Sub	694	G=1.000	C=0.000
KOREAN population from KRGDB	KOREAN	Study-wide	2922	G=0.9928	A=0.0014, C=0.0058
CNV burdens in cranial meningiomas	Global	Study-wide	790	G=0.997	C=0.003
CNV burdens in cranial meningiomas	CRM	Sub	790	G=0.997	C=0.003
A Vietnamese Genetic Variation Database	Global	Study-wide	216	G=0.991	C=0.009
SGDP_PRJ	Global	Study-wide	4	G=0.5	C=0.5

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.8753021G>A
GRCh38.p14 chr 3	NC_000003.12:g.8753021G>C
GRCh37.p13 chr 3	NC_000003.11:g.8794707G>A
GRCh37.p13 chr 3	NC_000003.11:g.8794707G>C
CAV3 RefSeqGene (LRG_329)	NG_008797.2:g.24212G>A
CAV3 RefSeqGene (LRG_329)	NG_008797.2:g.24212G>C

Gene: OXTR, oxytocin receptor (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
OXTR transcript variant 5	NM_001354656.3:c.1126C>T	R [CGC] > C [TGC]	Coding Sequence Variant
oxytocin receptor	NP_001341585.1:p.Arg376Cys	R (Arg) > C (Cys)	Missense Variant
OXTR transcript variant 5	NM_001354656.3:c.1126C>G	R [CGC] > G [GGC]	Coding Sequence Variant
oxytocin receptor	NP_001341585.1:p.Arg376Gly	R (Arg) > G (Gly)	Missense Variant
OXTR transcript variant 2	NM_001354653.2:c.1126C>T	R [CGC] > C [TGC]	Coding Sequence Variant
oxytocin receptor	NP_001341582.1:p.Arg376Cys	R (Arg) > C (Cys)	Missense Variant
OXTR transcript variant 2	NM_001354653.2:c.1126C>G	R [CGC] > G [GGC]	Coding Sequence Variant
oxytocin receptor	NP_001341582.1:p.Arg376Gly	R (Arg) > G (Gly)	Missense Variant
OXTR transcript variant 3	NM_001354654.2:c.1126C>T	R [CGC] > C [TGC]	Coding Sequence Variant
oxytocin receptor	NP_001341583.1:p.Arg376Cys	R (Arg) > C (Cys)	Missense Variant
OXTR transcript variant 3	NM_001354654.2:c.1126C>G	R [CGC] > G [GGC]	Coding Sequence Variant
oxytocin receptor	NP_001341583.1:p.Arg376Gly	R (Arg) > G (Gly)	Missense Variant
OXTR transcript variant 4	NM_001354655.2:c.1126C>T	R [CGC] > C [TGC]	Coding Sequence Variant
oxytocin receptor	NP_001341584.1:p.Arg376Cys	R (Arg) > C (Cys)	Missense Variant
OXTR transcript variant 4	NM_001354655.2:c.1126C>G	R [CGC] > G [GGC]	Coding Sequence Variant
oxytocin receptor	NP_001341584.1:p.Arg376Gly	R (Arg) > G (Gly)	Missense Variant
OXTR transcript variant 1	NM_000916.4:c.1126C>T	R [CGC] > C [TGC]	Coding Sequence Variant
oxytocin receptor	NP_000907.2:p.Arg376Cys	R (Arg) > C (Cys)	Missense Variant
OXTR transcript variant 1	NM_000916.4:c.1126C>G	R [CGC] > G [GGC]	Coding Sequence Variant
oxytocin receptor	NP_000907.2:p.Arg376Gly	R (Arg) > G (Gly)	Missense Variant
OXTR transcript variant X1	XR_007095681.1:n.1747C>T	N/A	Non Coding Transcript Variant
OXTR transcript variant X1	XR_007095681.1:n.1747C>G	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	G=	A	C
GRCh38.p14 chr 3	NC_000003.12:g.8753021=	NC_000003.12:g.8753021G>A	NC_000003.12:g.8753021G>C
GRCh37.p13 chr 3	NC_000003.11:g.8794707=	NC_000003.11:g.8794707G>A	NC_000003.11:g.8794707G>C
CAV3 RefSeqGene (LRG_329)	NG_008797.2:g.24212=	NG_008797.2:g.24212G>A	NG_008797.2:g.24212G>C
OXTR transcript variant 1	NM_000916.4:c.1126=	NM_000916.4:c.1126C>T	NM_000916.4:c.1126C>G
OXTR transcript variant 1	NM_000916.3:c.1126=	NM_000916.3:c.1126C>T	NM_000916.3:c.1126C>G
OXTR transcript variant 5	NM_001354656.3:c.1126=	NM_001354656.3:c.1126C>T	NM_001354656.3:c.1126C>G
OXTR transcript variant 5	NM_001354656.2:c.1126=	NM_001354656.2:c.1126C>T	NM_001354656.2:c.1126C>G
OXTR transcript variant 5	NM_001354656.1:c.1126=	NM_001354656.1:c.1126C>T	NM_001354656.1:c.1126C>G
OXTR transcript variant 3	NM_001354654.2:c.1126=	NM_001354654.2:c.1126C>T	NM_001354654.2:c.1126C>G
OXTR transcript variant 3	NM_001354654.1:c.1126=	NM_001354654.1:c.1126C>T	NM_001354654.1:c.1126C>G
OXTR transcript variant 2	NM_001354653.2:c.1126=	NM_001354653.2:c.1126C>T	NM_001354653.2:c.1126C>G
OXTR transcript variant 2	NM_001354653.1:c.1126=	NM_001354653.1:c.1126C>T	NM_001354653.1:c.1126C>G
OXTR transcript variant 4	NM_001354655.2:c.1126=	NM_001354655.2:c.1126C>T	NM_001354655.2:c.1126C>G
OXTR transcript variant 4	NM_001354655.1:c.1126=	NM_001354655.1:c.1126C>T	NM_001354655.1:c.1126C>G
OXTR transcript variant X1	XR_007095681.1:n.1747=	XR_007095681.1:n.1747C>T	XR_007095681.1:n.1747C>G
oxytocin receptor	NP_000907.2:p.Arg376=	NP_000907.2:p.Arg376Cys	NP_000907.2:p.Arg376Gly
oxytocin receptor	NP_001341585.1:p.Arg376=	NP_001341585.1:p.Arg376Cys	NP_001341585.1:p.Arg376Gly
oxytocin receptor	NP_001341583.1:p.Arg376=	NP_001341583.1:p.Arg376Cys	NP_001341583.1:p.Arg376Gly
oxytocin receptor	NP_001341582.1:p.Arg376=	NP_001341582.1:p.Arg376Cys	NP_001341582.1:p.Arg376Gly
oxytocin receptor	NP_001341584.1:p.Arg376=	NP_001341584.1:p.Arg376Cys	NP_001341584.1:p.Arg376Gly

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#.

85 SubSNP, 21 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	RIKENSNPRC	ss49848820	Mar 14, 2006 (126)
2	ILLUMINA	ss154260645	Dec 01, 2009 (131)
3	ILLUMINA	ss159437254	Dec 01, 2009 (131)
4	ILLUMINA	ss160624987	Dec 01, 2009 (131)
5	ILLUMINA	ss173596280	Jul 04, 2010 (132)
6	1000GENOMES	ss330484704	May 09, 2011 (134)
7	ILLUMINA	ss480787725	May 04, 2012 (137)
8	ILLUMINA	ss480803457	May 04, 2012 (137)
9	ILLUMINA	ss481714678	Sep 08, 2015 (146)
10	ILLUMINA	ss485188650	May 04, 2012 (137)
11	1000GENOMES	ss489863819	May 04, 2012 (137)
12	GSK-GENETICS	ss491266424	May 04, 2012 (137)
13	EXOME_CHIP	ss491335155	May 04, 2012 (137)
14	ILLUMINA	ss537177349	Sep 08, 2015 (146)
15	ILLUMINA	ss778718991	Sep 08, 2015 (146)
16	ILLUMINA	ss780789876	Sep 08, 2015 (146)
17	ILLUMINA	ss783040388	Sep 08, 2015 (146)
18	ILLUMINA	ss783470666	Sep 08, 2015 (146)
19	ILLUMINA	ss783999700	Sep 08, 2015 (146)
20	ILLUMINA	ss832298123	Sep 08, 2015 (146)
21	ILLUMINA	ss832948842	Jul 13, 2019 (153)
22	ILLUMINA	ss834178367	Sep 08, 2015 (146)
23	JMKIDD_LAB	ss1067447947	Aug 21, 2014 (142)
24	JMKIDD_LAB	ss1070160667	Aug 21, 2014 (142)
25	1000GENOMES	ss1302724700	Aug 21, 2014 (142)
26	EVA_EXAC	ss1686852788	Apr 01, 2015 (144)
27	EVA_EXAC	ss1686852789	Apr 01, 2015 (144)
28	ILLUMINA	ss1752486602	Sep 08, 2015 (146)
29	ILLUMINA	ss1752486603	Sep 08, 2015 (146)
30	ILLUMINA	ss1917762921	Feb 12, 2016 (147)
31	ILLUMINA	ss1946073860	Feb 12, 2016 (147)
32	ILLUMINA	ss1958534916	Feb 12, 2016 (147)
33	HUMAN_LONGEVITY	ss2248922105	Dec 20, 2016 (150)
34	ILLUMINA	ss2633908584	Nov 08, 2017 (151)
35	ILLUMINA	ss2710964671	Nov 08, 2017 (151)
36	GNOMAD	ss2733516263	Nov 08, 2017 (151)
37	GNOMAD	ss2746938692	Nov 08, 2017 (151)
38	GNOMAD	ss2789315611	Nov 08, 2017 (151)
39	AFFY	ss2985246113	Nov 08, 2017 (151)
40	AFFY	ss2985865335	Nov 08, 2017 (151)
41	ILLUMINA	ss3022209263	Nov 08, 2017 (151)
42	ILLUMINA	ss3628584974	Oct 11, 2018 (152)
43	ILLUMINA	ss3628584975	Oct 11, 2018 (152)
44	ILLUMINA	ss3631857417	Oct 11, 2018 (152)
45	ILLUMINA	ss3633997557	Oct 11, 2018 (152)
46	ILLUMINA	ss3634878983	Oct 11, 2018 (152)
47	ILLUMINA	ss3634878984	Oct 11, 2018 (152)
48	ILLUMINA	ss3635681775	Oct 11, 2018 (152)
49	ILLUMINA	ss3636575228	Oct 11, 2018 (152)
50	ILLUMINA	ss3637434072	Oct 11, 2018 (152)
51	ILLUMINA	ss3638395755	Oct 11, 2018 (152)
52	ILLUMINA	ss3640586286	Oct 11, 2018 (152)
53	ILLUMINA	ss3640586287	Oct 11, 2018 (152)
54	ILLUMINA	ss3644806394	Oct 11, 2018 (152)
55	ILLUMINA	ss3652675150	Oct 11, 2018 (152)
56	ILLUMINA	ss3654014606	Oct 11, 2018 (152)
57	ILLUMINA	ss3725988074	Jul 13, 2019 (153)
58	ILLUMINA	ss3744505748	Jul 13, 2019 (153)
59	ILLUMINA	ss3745178794	Jul 13, 2019 (153)
60	ILLUMINA	ss3745178795	Jul 13, 2019 (153)
61	EVA	ss3759636086	Jul 13, 2019 (153)
62	PAGE_CC	ss3771009073	Jul 13, 2019 (153)
63	ILLUMINA	ss3772674599	Jul 13, 2019 (153)
64	ILLUMINA	ss3772674600	Jul 13, 2019 (153)
65	KHV_HUMAN_GENOMES	ss3802787869	Jul 13, 2019 (153)
66	SGDP_PRJ	ss3855186386	Apr 25, 2020 (154)
67	KRGDB	ss3900953417	Apr 25, 2020 (154)
68	KOGIC	ss3950623348	Apr 25, 2020 (154)
69	KOGIC	ss3950623349	Apr 25, 2020 (154)
70	EVA	ss3984502588	Apr 26, 2021 (155)
71	TOPMED	ss4553566193	Apr 26, 2021 (155)
72	TOPMED	ss4553566194	Apr 26, 2021 (155)
73	TOMMO_GENOMICS	ss5157709658	Apr 26, 2021 (155)
74	TOMMO_GENOMICS	ss5157709659	Apr 26, 2021 (155)
75	EVA	ss5236993599	Apr 26, 2021 (155)
76	1000G_HIGH_COVERAGE	ss5252980766	Oct 13, 2022 (156)
77	EVA	ss5314831914	Oct 13, 2022 (156)
78	EVA	ss5337766309	Oct 13, 2022 (156)
79	1000G_HIGH_COVERAGE	ss5530780376	Oct 13, 2022 (156)
80	SANFORD_IMAGENETICS	ss5631504479	Oct 13, 2022 (156)
81	TOMMO_GENOMICS	ss5688951076	Oct 13, 2022 (156)
82	TOMMO_GENOMICS	ss5688951077	Oct 13, 2022 (156)
83	EVA	ss5847952720	Oct 13, 2022 (156)
84	EVA	ss5867551370	Oct 13, 2022 (156)
85	EVA	ss5959762173	Oct 13, 2022 (156)
86	1000Genomes	NC_000003.11 - 8794707	Oct 11, 2018 (152)
87	1000Genomes_30x	NC_000003.12 - 8753021	Oct 13, 2022 (156)
88	ExAC Submission ignored due to conflicting rows: Row 6765899 (NC_000003.11:8794706:G:G 119589/119626, NC_000003.11:8794706:G:C 37/119626) Row 6765900 (NC_000003.11:8794706:G:G 119623/119626, NC_000003.11:8794706:G:A 3/119626)	-	Oct 11, 2018 (152)
89	ExAC Submission ignored due to conflicting rows: Row 6765899 (NC_000003.11:8794706:G:G 119589/119626, NC_000003.11:8794706:G:C 37/119626) Row 6765900 (NC_000003.11:8794706:G:G 119623/119626, NC_000003.11:8794706:G:A 3/119626)	-	Oct 11, 2018 (152)
90	gnomAD - Genomes	NC_000003.12 - 8753021	Apr 26, 2021 (155)
91	gnomAD - Exomes Submission ignored due to conflicting rows: Row 2586997 (NC_000003.11:8794706:G:G 250402/250406, NC_000003.11:8794706:G:A 4/250406) Row 2586998 (NC_000003.11:8794706:G:G 250320/250406, NC_000003.11:8794706:G:C 86/250406)	-	Jul 13, 2019 (153)
92	gnomAD - Exomes Submission ignored due to conflicting rows: Row 2586997 (NC_000003.11:8794706:G:G 250402/250406, NC_000003.11:8794706:G:A 4/250406) Row 2586998 (NC_000003.11:8794706:G:G 250320/250406, NC_000003.11:8794706:G:C 86/250406)	-	Jul 13, 2019 (153)
93	KOREAN population from KRGDB	NC_000003.11 - 8794707	Apr 25, 2020 (154)
94	Korean Genome Project Submission ignored due to conflicting rows: Row 7001349 (NC_000003.12:8753020:G:C 12/1832) Row 7001350 (NC_000003.12:8753020:G:A 2/1832)	-	Apr 25, 2020 (154)
95	Korean Genome Project Submission ignored due to conflicting rows: Row 7001349 (NC_000003.12:8753020:G:C 12/1832) Row 7001350 (NC_000003.12:8753020:G:A 2/1832)	-	Apr 25, 2020 (154)
96	The PAGE Study	NC_000003.12 - 8753021	Jul 13, 2019 (153)
97	CNV burdens in cranial meningiomas	NC_000003.11 - 8794707	Apr 26, 2021 (155)
98	SGDP_PRJ	NC_000003.11 - 8794707	Apr 25, 2020 (154)
99	8.3KJPN Submission ignored due to conflicting rows: Row 15678965 (NC_000003.11:8794706:G:C 176/16760) Row 15678966 (NC_000003.11:8794706:G:A 31/16760)	-	Apr 26, 2021 (155)
100	8.3KJPN Submission ignored due to conflicting rows: Row 15678965 (NC_000003.11:8794706:G:C 176/16760) Row 15678966 (NC_000003.11:8794706:G:A 31/16760)	-	Apr 26, 2021 (155)
101	14KJPN Submission ignored due to conflicting rows: Row 22788180 (NC_000003.12:8753020:G:A 56/28258) Row 22788181 (NC_000003.12:8753020:G:C 303/28258)	-	Oct 13, 2022 (156)
102	14KJPN Submission ignored due to conflicting rows: Row 22788180 (NC_000003.12:8753020:G:A 56/28258) Row 22788181 (NC_000003.12:8753020:G:C 303/28258)	-	Oct 13, 2022 (156)
103	TopMed Submission ignored due to conflicting rows: Row 390943748 (NC_000003.12:8753020:G:A 4/264690) Row 390943749 (NC_000003.12:8753020:G:C 50/264690)	-	Apr 26, 2021 (155)
104	TopMed Submission ignored due to conflicting rows: Row 390943748 (NC_000003.12:8753020:G:A 4/264690) Row 390943749 (NC_000003.12:8753020:G:C 50/264690)	-	Apr 26, 2021 (155)
105	A Vietnamese Genetic Variation Database	NC_000003.11 - 8794707	Jul 13, 2019 (153)
106	ALFA	NC_000003.12 - 8753021	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).

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss491266424	NC_000003.10:8769706:G:A	NC_000003.12:8753020:G:A	(self)
8130811, ss1686852789, ss2733516263, ss3900953417, ss5157709659	NC_000003.11:8794706:G:A	NC_000003.12:8753020:G:A	(self)
18306311, 2869379499, ss2248922105, ss3950623349, ss4553566193, ss5530780376, ss5688951076	NC_000003.12:8753020:G:A	NC_000003.12:8753020:G:A	(self)
ss480787725, ss491266424	NC_000003.10:8769706:G:C	NC_000003.12:8753020:G:C	(self)
13866880, 8130811, 51930, 7203366, 1673707, ss330484704, ss480803457, ss481714678, ss485188650, ss489863819, ss491335155, ss537177349, ss778718991, ss780789876, ss783040388, ss783470666, ss783999700, ss832298123, ss832948842, ss834178367, ss1067447947, ss1070160667, ss1302724700, ss1686852788, ss1752486602, ss1752486603, ss1917762921, ss1946073860, ss1958534916, ss2633908584, ss2710964671, ss2733516263, ss2746938692, ss2789315611, ss2985246113, ss2985865335, ss3022209263, ss3628584974, ss3628584975, ss3631857417, ss3633997557, ss3634878983, ss3634878984, ss3635681775, ss3636575228, ss3637434072, ss3638395755, ss3640586286, ss3640586287, ss3644806394, ss3652675150, ss3654014606, ss3744505748, ss3745178794, ss3745178795, ss3759636086, ss3772674599, ss3772674600, ss3855186386, ss3900953417, ss3984502588, ss5157709658, ss5314831914, ss5337766309, ss5631504479, ss5847952720, ss5959762173	NC_000003.11:8794706:G:C	NC_000003.12:8753020:G:C	(self)
18306311, 98485933, 230542, 2869379499, ss2248922105, ss3725988074, ss3771009073, ss3802787869, ss3950623348, ss4553566194, ss5236993599, ss5252980766, ss5530780376, ss5688951077, ss5867551370	NC_000003.12:8753020:G:C	NC_000003.12:8753020:G:C	(self)
ss49848820, ss154260645, ss159437254, ss160624987, ss173596280	NT_022517.18:8734706:G:C	NC_000003.12:8753020:G:C	(self)

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

2 citations for rs35062132

PMID	Title	Author	Year	Journal
24836510	Resequencing and association analysis of OXTR with autism spectrum disorder in a Japanese population.	Egawa J et al.	2015	Psychiatry and clinical neurosciences
27421662	Functional characterization of an oxytocin receptor gene variant (rs2268498) previously associated with social cognition by expression analysis in vitro and in human brain biopsy.	Reuter M et al.	2017	Social neuroscience

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

rs35062132