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dbSNP Short Genetic Variations

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.

rs53576

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr3:8762685 (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
A>G / A>T
Variation Type
SNV Single Nucleotide Variation
Frequency
A=0.306872 (81226/264690, TOPMED)
A=0.309437 (43359/140122, GnomAD)
A=0.32646 (24474/74968, ALFA) (+ 18 more)
G=0.37342 (10552/28258, 14KJPN)
G=0.37548 (6293/16760, 8.3KJPN)
A=0.3784 (2423/6404, 1000G_30x)
A=0.3894 (1950/5008, 1000G)
A=0.3641 (1631/4480, Estonian)
A=0.3238 (1248/3854, ALSPAC)
A=0.3223 (1195/3708, TWINSUK)
G=0.3372 (988/2930, KOREAN)
A=0.343 (342/998, GoNL)
G=0.313 (247/788, PRJEB37584)
A=0.340 (204/600, NorthernSweden)
A=0.282 (120/426, SGDP_PRJ)
A=0.324 (70/216, Qatari)
G=0.310 (67/216, Vietnamese)
A=0.35 (14/40, GENOME_DK)
A=0.36 (13/36, Siberian)
A=0.50 (14/28, Ancient Sardinia)
G=0.50 (14/28, Ancient Sardinia)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
OXTR : Intron Variant
Publications
234 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 74968 A=0.32646 G=0.67354, T=0.00000
European Sub 62252 A=0.32577 G=0.67423, T=0.00000
African Sub 4144 A=0.2379 G=0.7621, T=0.0000
African Others Sub 154 A=0.214 G=0.786, T=0.000
African American Sub 3990 A=0.2388 G=0.7612, T=0.0000
Asian Sub 188 A=0.559 G=0.441, T=0.000
East Asian Sub 148 A=0.581 G=0.419, T=0.000
Other Asian Sub 40 A=0.47 G=0.53, T=0.00
Latin American 1 Sub 242 A=0.256 G=0.744, T=0.000
Latin American 2 Sub 1236 A=0.3657 G=0.6343, T=0.0000
South Asian Sub 4932 A=0.3944 G=0.6056, T=0.0000
Other Sub 1974 A=0.3262 G=0.6738, T=0.0000


Help

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
TopMed Global Study-wide 264690 A=0.306872 G=0.693128
gnomAD - Genomes Global Study-wide 140122 A=0.309437 G=0.690563
gnomAD - Genomes European Sub 75880 A=0.33861 G=0.66139
gnomAD - Genomes African Sub 41998 A=0.22013 G=0.77987
gnomAD - Genomes American Sub 13648 A=0.34525 G=0.65475
gnomAD - Genomes Ashkenazi Jewish Sub 3316 A=0.2952 G=0.7048
gnomAD - Genomes East Asian Sub 3128 A=0.6541 G=0.3459
gnomAD - Genomes Other Sub 2152 A=0.3174 G=0.6826
Allele Frequency Aggregator Total Global 74968 A=0.32646 G=0.67354, T=0.00000
Allele Frequency Aggregator European Sub 62252 A=0.32577 G=0.67423, T=0.00000
Allele Frequency Aggregator South Asian Sub 4932 A=0.3944 G=0.6056, T=0.0000
Allele Frequency Aggregator African Sub 4144 A=0.2379 G=0.7621, T=0.0000
Allele Frequency Aggregator Other Sub 1974 A=0.3262 G=0.6738, T=0.0000
Allele Frequency Aggregator Latin American 2 Sub 1236 A=0.3657 G=0.6343, T=0.0000
Allele Frequency Aggregator Latin American 1 Sub 242 A=0.256 G=0.744, T=0.000
Allele Frequency Aggregator Asian Sub 188 A=0.559 G=0.441, T=0.000
14KJPN JAPANESE Study-wide 28258 A=0.62658 G=0.37342
8.3KJPN JAPANESE Study-wide 16760 A=0.62452 G=0.37548
1000Genomes_30x Global Study-wide 6404 A=0.3784 G=0.6216
1000Genomes_30x African Sub 1786 A=0.1870 G=0.8130
1000Genomes_30x Europe Sub 1266 A=0.3428 G=0.6572
1000Genomes_30x South Asian Sub 1202 A=0.4476 G=0.5524
1000Genomes_30x East Asian Sub 1170 A=0.6573 G=0.3427
1000Genomes_30x American Sub 980 A=0.355 G=0.645
1000Genomes Global Study-wide 5008 A=0.3894 G=0.6106
1000Genomes African Sub 1322 A=0.1936 G=0.8064
1000Genomes East Asian Sub 1008 A=0.6498 G=0.3502
1000Genomes Europe Sub 1006 A=0.3509 G=0.6491
1000Genomes South Asian Sub 978 A=0.449 G=0.551
1000Genomes American Sub 694 A=0.356 G=0.644
Genetic variation in the Estonian population Estonian Study-wide 4480 A=0.3641 G=0.6359
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 A=0.3238 G=0.6762
UK 10K study - Twins TWIN COHORT Study-wide 3708 A=0.3223 G=0.6777
KOREAN population from KRGDB KOREAN Study-wide 2930 A=0.6628 G=0.3372, T=0.0000
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 A=0.343 G=0.657
CNV burdens in cranial meningiomas Global Study-wide 788 A=0.687 G=0.313
CNV burdens in cranial meningiomas CRM Sub 788 A=0.687 G=0.313
Northern Sweden ACPOP Study-wide 600 A=0.340 G=0.660
SGDP_PRJ Global Study-wide 426 A=0.282 G=0.718
Qatari Global Study-wide 216 A=0.324 G=0.676
A Vietnamese Genetic Variation Database Global Study-wide 216 A=0.690 G=0.310
The Danish reference pan genome Danish Study-wide 40 A=0.35 G=0.65
Siberian Global Study-wide 36 A=0.36 G=0.64
Ancient Sardinia genome-wide 1240k capture data generation and analysis Global Study-wide 28 A=0.50 G=0.50
Help

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.8762685A>G
GRCh38.p14 chr 3 NC_000003.12:g.8762685A>T
GRCh37.p13 chr 3 NC_000003.11:g.8804371A>G
GRCh37.p13 chr 3 NC_000003.11:g.8804371A>T
CAV3 RefSeqGene (LRG_329) NG_008797.2:g.33876A>G
CAV3 RefSeqGene (LRG_329) NG_008797.2:g.33876A>T
Gene: OXTR, oxytocin receptor (minus strand)
Molecule type Change Amino acid[Codon] SO Term
OXTR transcript variant 1 NM_000916.4:c.922+4581T>C N/A Intron Variant
OXTR transcript variant 2 NM_001354653.2:c.922+4581…

NM_001354653.2:c.922+4581T>C

N/A Intron Variant
OXTR transcript variant 3 NM_001354654.2:c.922+4581…

NM_001354654.2:c.922+4581T>C

N/A Intron Variant
OXTR transcript variant 4 NM_001354655.2:c.922+4581…

NM_001354655.2:c.922+4581T>C

N/A Intron Variant
OXTR transcript variant 5 NM_001354656.3:c.922+4581…

NM_001354656.3:c.922+4581T>C

N/A Intron Variant
OXTR transcript variant X1 XR_007095681.1:n. N/A Intron Variant
Help

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
Help

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 A= G T
GRCh38.p14 chr 3 NC_000003.12:g.8762685= NC_000003.12:g.8762685A>G NC_000003.12:g.8762685A>T
GRCh37.p13 chr 3 NC_000003.11:g.8804371= NC_000003.11:g.8804371A>G NC_000003.11:g.8804371A>T
CAV3 RefSeqGene (LRG_329) NG_008797.2:g.33876= NG_008797.2:g.33876A>G NG_008797.2:g.33876A>T
OXTR transcript variant 1 NM_000916.3:c.922+4581= NM_000916.3:c.922+4581T>C NM_000916.3:c.922+4581T>A
OXTR transcript variant 1 NM_000916.4:c.922+4581= NM_000916.4:c.922+4581T>C NM_000916.4:c.922+4581T>A
OXTR transcript variant 2 NM_001354653.2:c.922+4581= NM_001354653.2:c.922+4581T>C NM_001354653.2:c.922+4581T>A
OXTR transcript variant 3 NM_001354654.2:c.922+4581= NM_001354654.2:c.922+4581T>C NM_001354654.2:c.922+4581T>A
OXTR transcript variant 4 NM_001354655.2:c.922+4581= NM_001354655.2:c.922+4581T>C NM_001354655.2:c.922+4581T>A
OXTR transcript variant 5 NM_001354656.3:c.922+4581= NM_001354656.3:c.922+4581T>C NM_001354656.3:c.922+4581T>A
Help

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#.

103 SubSNP, 20 Frequency submissions
No Submitter Submission ID Date (Build)
1 TSC-CSHL ss59712 Oct 04, 2000 (86)
2 KWOK ss306658 Jul 10, 2000 (79)
3 KWOK ss439098 Jul 12, 2000 (87)
4 SC_JCM ss528564 Jul 16, 2000 (87)
5 KWOK ss1014572 Oct 04, 2000 (86)
6 KWOK ss1055347 Oct 04, 2000 (86)
7 KWOK ss1652914 Oct 18, 2000 (87)
8 SC_JCM ss5673592 Feb 20, 2003 (111)
9 BCM_SSAHASNP ss14183444 Dec 05, 2003 (119)
10 CSHL-HAPMAP ss16948813 Feb 27, 2004 (120)
11 SSAHASNP ss21950419 Apr 05, 2004 (121)
12 ABI ss44461127 Mar 13, 2006 (126)
13 PERLEGEN ss46541669 Mar 13, 2006 (126)
14 RIKENSNPRC ss49848815 Mar 13, 2006 (126)
15 HGSV ss78851103 Dec 07, 2007 (129)
16 HGSV ss84951144 Dec 16, 2007 (130)
17 BCMHGSC_JDW ss91992564 Mar 24, 2008 (129)
18 HUMANGENOME_JCVI ss99074608 Feb 06, 2009 (130)
19 BGI ss103897889 Dec 01, 2009 (131)
20 1000GENOMES ss111225319 Jan 25, 2009 (130)
21 1000GENOMES ss112052328 Jan 25, 2009 (130)
22 ILLUMINA-UK ss116967912 Feb 14, 2009 (130)
23 ENSEMBL ss135225564 Dec 01, 2009 (131)
24 ENSEMBL ss138713663 Dec 01, 2009 (131)
25 ILLUMINA ss154337722 Dec 01, 2009 (131)
26 GMI ss155083237 Dec 01, 2009 (131)
27 ILLUMINA ss159514304 Dec 01, 2009 (131)
28 COMPLETE_GENOMICS ss161915046 Jul 04, 2010 (132)
29 COMPLETE_GENOMICS ss163085984 Jul 04, 2010 (132)
30 COMPLETE_GENOMICS ss166129391 Jul 04, 2010 (132)
31 ILLUMINA ss173915915 Jul 04, 2010 (132)
32 BUSHMAN ss202109412 Jul 04, 2010 (132)
33 BCM-HGSC-SUB ss206134681 Jul 04, 2010 (132)
34 1000GENOMES ss219970775 Jul 14, 2010 (132)
35 1000GENOMES ss231700317 Jul 14, 2010 (132)
36 1000GENOMES ss239135799 Jul 15, 2010 (132)
37 BL ss252921855 May 09, 2011 (134)
38 GMI ss277006576 May 04, 2012 (137)
39 GMI ss284591708 Apr 25, 2013 (138)
40 PJP ss292858691 May 09, 2011 (134)
41 ILLUMINA ss479382349 May 04, 2012 (137)
42 ILLUMINA ss484649902 May 04, 2012 (137)
43 ILLUMINA ss532941640 Sep 08, 2015 (146)
44 TISHKOFF ss556413349 Apr 25, 2013 (138)
45 SSMP ss650078333 Apr 25, 2013 (138)
46 ILLUMINA ss779576289 Sep 08, 2015 (146)
47 ILLUMINA ss780967562 Sep 08, 2015 (146)
48 ILLUMINA ss833025600 Jul 13, 2019 (153)
49 ILLUMINA ss835047738 Sep 08, 2015 (146)
50 EVA-GONL ss978252171 Aug 21, 2014 (142)
51 JMKIDD_LAB ss1070160726 Aug 21, 2014 (142)
52 1000GENOMES ss1302725027 Aug 21, 2014 (142)
53 DDI ss1429324856 Apr 01, 2015 (144)
54 EVA_GENOME_DK ss1579837623 Apr 01, 2015 (144)
55 EVA_DECODE ss1587712276 Apr 01, 2015 (144)
56 EVA_UK10K_ALSPAC ss1606373064 Apr 01, 2015 (144)
57 EVA_UK10K_TWINSUK ss1649367097 Apr 01, 2015 (144)
58 HAMMER_LAB ss1798826805 Sep 08, 2015 (146)
59 WEILL_CORNELL_DGM ss1921503730 Feb 12, 2016 (147)
60 GENOMED ss1969318795 Jul 19, 2016 (147)
61 JJLAB ss2021304681 Sep 14, 2016 (149)
62 USC_VALOUEV ss2149371904 Dec 20, 2016 (150)
63 HUMAN_LONGEVITY ss2248922741 Dec 20, 2016 (150)
64 SYSTEMSBIOZJU ss2625152856 Nov 08, 2017 (151)
65 ILLUMINA ss2633908611 Nov 08, 2017 (151)
66 GRF ss2704730737 Nov 08, 2017 (151)
67 GNOMAD ss2789316395 Nov 08, 2017 (151)
68 AFFY ss2985865383 Nov 08, 2017 (151)
69 SWEGEN ss2991798893 Nov 08, 2017 (151)
70 BIOINF_KMB_FNS_UNIBA ss3024415283 Nov 08, 2017 (151)
71 CSHL ss3344875995 Nov 08, 2017 (151)
72 ILLUMINA ss3628585015 Oct 11, 2018 (152)
73 ILLUMINA ss3631857441 Oct 11, 2018 (152)
74 ILLUMINA ss3638395767 Oct 11, 2018 (152)
75 ILLUMINA ss3642232861 Oct 11, 2018 (152)
76 URBANLAB ss3647336470 Oct 11, 2018 (152)
77 EGCUT_WGS ss3659698815 Jul 13, 2019 (153)
78 EVA_DECODE ss3708598227 Jul 13, 2019 (153)
79 ACPOP ss3729615751 Jul 13, 2019 (153)
80 EVA ss3759636198 Jul 13, 2019 (153)
81 PACBIO ss3784229979 Jul 13, 2019 (153)
82 PACBIO ss3789759450 Jul 13, 2019 (153)
83 PACBIO ss3794633193 Jul 13, 2019 (153)
84 KHV_HUMAN_GENOMES ss3802787969 Jul 13, 2019 (153)
85 EVA ss3827651703 Apr 25, 2020 (154)
86 SGDP_PRJ ss3855186553 Apr 25, 2020 (154)
87 KRGDB ss3900953568 Apr 25, 2020 (154)
88 EVA ss3984502600 Apr 26, 2021 (155)
89 EVA ss3984971607 Apr 26, 2021 (155)
90 TOPMED ss4553568730 Apr 26, 2021 (155)
91 TOMMO_GENOMICS ss5157709959 Apr 26, 2021 (155)
92 1000G_HIGH_COVERAGE ss5252981028 Oct 13, 2022 (156)
93 EVA ss5314831936 Oct 13, 2022 (156)
94 EVA ss5337766837 Oct 13, 2022 (156)
95 HUGCELL_USP ss5452489490 Oct 13, 2022 (156)
96 1000G_HIGH_COVERAGE ss5530780795 Oct 13, 2022 (156)
97 SANFORD_IMAGENETICS ss5631504633 Oct 13, 2022 (156)
98 TOMMO_GENOMICS ss5688951462 Oct 13, 2022 (156)
99 YY_MCH ss5803464059 Oct 13, 2022 (156)
100 EVA ss5825319992 Oct 13, 2022 (156)
101 EVA ss5853482349 Oct 13, 2022 (156)
102 EVA ss5867551703 Oct 13, 2022 (156)
103 EVA ss5959762353 Oct 13, 2022 (156)
104 1000Genomes NC_000003.11 - 8804371 Oct 11, 2018 (152)
105 1000Genomes_30x NC_000003.12 - 8762685 Oct 13, 2022 (156)
106 The Avon Longitudinal Study of Parents and Children NC_000003.11 - 8804371 Oct 11, 2018 (152)
107 Genetic variation in the Estonian population NC_000003.11 - 8804371 Oct 11, 2018 (152)
108 The Danish reference pan genome NC_000003.11 - 8804371 Apr 25, 2020 (154)
109 gnomAD - Genomes NC_000003.12 - 8762685 Apr 26, 2021 (155)
110 Genome of the Netherlands Release 5 NC_000003.11 - 8804371 Apr 25, 2020 (154)
111 KOREAN population from KRGDB NC_000003.11 - 8804371 Apr 25, 2020 (154)
112 Northern Sweden NC_000003.11 - 8804371 Jul 13, 2019 (153)
113 Ancient Sardinia genome-wide 1240k capture data generation and analysis NC_000003.11 - 8804371 Apr 26, 2021 (155)
114 CNV burdens in cranial meningiomas NC_000003.11 - 8804371 Apr 26, 2021 (155)
115 Qatari NC_000003.11 - 8804371 Apr 25, 2020 (154)
116 SGDP_PRJ NC_000003.11 - 8804371 Apr 25, 2020 (154)
117 Siberian NC_000003.11 - 8804371 Apr 25, 2020 (154)
118 8.3KJPN NC_000003.11 - 8804371 Apr 26, 2021 (155)
119 14KJPN NC_000003.12 - 8762685 Oct 13, 2022 (156)
120 TopMed NC_000003.12 - 8762685 Apr 26, 2021 (155)
121 UK 10K study - Twins NC_000003.11 - 8804371 Oct 11, 2018 (152)
122 A Vietnamese Genetic Variation Database NC_000003.11 - 8804371 Jul 13, 2019 (153)
123 ALFA NC_000003.12 - 8762685 Apr 26, 2021 (155)
Help

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)
rs345116 Oct 23, 2000 (87)
rs61493474 May 26, 2008 (130)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
ss78851103, ss84951144 NC_000003.9:8779370:A:G NC_000003.12:8762684:A:G (self)
ss91992564, ss111225319, ss112052328, ss116967912, ss161915046, ss163085984, ss166129391, ss202109412, ss206134681, ss252921855, ss277006576, ss284591708, ss292858691, ss484649902, ss1587712276 NC_000003.10:8779370:A:G NC_000003.12:8762684:A:G (self)
13867212, 7686154, 5437063, 6002562, 3375552, 8130962, 2900616, 197534, 51942, 3545660, 7203533, 1888258, 15679266, 7686154, 1673758, ss219970775, ss231700317, ss239135799, ss479382349, ss532941640, ss556413349, ss650078333, ss779576289, ss780967562, ss833025600, ss835047738, ss978252171, ss1070160726, ss1302725027, ss1429324856, ss1579837623, ss1606373064, ss1649367097, ss1798826805, ss1921503730, ss1969318795, ss2021304681, ss2149371904, ss2625152856, ss2633908611, ss2704730737, ss2789316395, ss2985865383, ss2991798893, ss3344875995, ss3628585015, ss3631857441, ss3638395767, ss3642232861, ss3659698815, ss3729615751, ss3759636198, ss3784229979, ss3789759450, ss3794633193, ss3827651703, ss3855186553, ss3900953568, ss3984502600, ss3984971607, ss5157709959, ss5314831936, ss5337766837, ss5631504633, ss5825319992, ss5959762353 NC_000003.11:8804370:A:G NC_000003.12:8762684:A:G (self)
18306730, 98487949, 22788566, 390946285, 8607225291, ss2248922741, ss3024415283, ss3647336470, ss3708598227, ss3802787969, ss4553568730, ss5252981028, ss5452489490, ss5530780795, ss5688951462, ss5803464059, ss5853482349, ss5867551703 NC_000003.12:8762684:A:G NC_000003.12:8762684:A:G (self)
ss14183444, ss16948813, ss21950419 NT_022517.16:8744370:A:G NC_000003.12:8762684:A:G (self)
ss59712, ss306658, ss439098, ss528564, ss1014572, ss1055347, ss1652914, ss5673592, ss44461127, ss46541669, ss49848815, ss99074608, ss103897889, ss135225564, ss138713663, ss154337722, ss155083237, ss159514304, ss173915915 NT_022517.18:8744370:A:G NC_000003.12:8762684:A:G (self)
8130962, ss3900953568 NC_000003.11:8804370:A:T NC_000003.12:8762684:A:T (self)
8607225291 NC_000003.12:8762684:A:T NC_000003.12:8762684:A:T (self)
Help

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

234 citations for rs53576
PMID Title Author Year Journal
15992526 Positive association of the oxytocin receptor gene (OXTR) with autism in the Chinese Han population. Wu S et al. 2005 Biological psychiatry
17383819 Association of the oxytocin receptor gene (OXTR) in Caucasian children and adolescents with autism. Jacob S et al. 2007 Neuroscience letters
18687882 Genetic correlates of adult attachment style. Gillath O et al. 2008 Personality & social psychology bulletin
19015103 Oxytocin receptor (OXTR) and serotonin transporter (5-HTT) genes associated with observed parenting. Bakermans-Kranenburg MJ et al. 2008 Social cognitive and affective neuroscience
19376182 Associations between the oxytocin receptor gene (OXTR) and affect, loneliness and intelligence in normal subjects. Lucht MJ et al. 2009 Progress in neuro-psychopharmacology & biological psychiatry
19515497 Oxytocin receptor polymorphisms and adult attachment style in patients with depression. Costa B et al. 2009 Psychoneuroendocrinology
19934046 Oxytocin receptor genetic variation relates to empathy and stress reactivity in humans. Rodrigues SM et al. 2009 Proceedings of the National Academy of Sciences of the United States of America
20347913 Evidence that genetic variation in the oxytocin receptor (OXTR) gene influences social cognition in ADHD. Park J et al. 2010 Progress in neuro-psychopharmacology & biological psychiatry
20585395 No association between oxytocin receptor (OXTR) gene polymorphisms and experimentally elicited social preferences. Apicella CL et al. 2010 PloS one
20647384 A common allele in the oxytocin receptor gene (OXTR) impacts prosocial temperament and human hypothalamic-limbic structure and function. Tost H et al. 2010 Proceedings of the National Academy of Sciences of the United States of America
20724662 Culture, distress, and oxytocin receptor polymorphism (OXTR) interact to influence emotional support seeking. Kim HS et al. 2010 Proceedings of the National Academy of Sciences of the United States of America
21484202 Association of oxytocin receptor (OXTR) gene variants with multiple phenotype domains of autism spectrum disorder. Campbell DB et al. 2011 Journal of neurodevelopmental disorders
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33866050 Oxytocin system dysfunction in patients with treatment-resistant schizophrenia: Alterations of blood oxytocin levels and effect of a genetic variant of OXTR. Nakata Y et al. 2021 Journal of psychiatric research
33892530 The influence of rs53576 polymorphism in the oxytocin receptor (OXTR) gene on empathy in healthy adults by subtype and ethnicity: a systematic review and meta-analysis. Chander RJ et al. 2022 Reviews in the neurosciences
33919740 Recalled Parental Bonding Interacts with Oxytocin Receptor Gene Polymorphism in Modulating Anxiety and Avoidance in Adult Relationships. Cataldo I et al. 2021 Brain sciences
34023733 Associations between oxytocin and empathy in humans: A systematic literature review. Barchi-Ferreira AM et al. 2021 Psychoneuroendocrinology
34091593 Oxytocin receptor gene polymorphism and low serum oxytocin level are associated with hyperphagia and obesity in adolescents. Çatli G et al. 2021 International journal of obesity (2005)
34118640 OXTR moderates adverse childhood experiences on depressive symptoms among incarcerated males. Zhang J et al. 2021 Journal of psychiatric research
34144447 Gene-environment interaction: Oxytocin receptor (OXTR) polymorphisms and parenting style as potential predictors for depressive symptoms. Keijser R et al. 2021 Psychiatry research
34256847 Review of eating disorders and oxytocin receptor polymorphisms. Burmester V et al. 2021 Journal of eating disorders
34301983 Randomized clinical trial shows no substantial modulation of empathy-related neural activation by intranasal oxytocin in autism. Mayer AV et al. 2021 Scientific reports
34371296 Genetic markers of the stress generation model: A systematic review. Bahji A et al. 2021 Psychiatry research
34611556 The relation between oxytocin receptor gene polymorphisms, adult attachment and Instagram sociability: An exploratory analysis. Carollo A et al. 2021 Heliyon
34661982 Oxytocin receptor polymorphism influences characterization of harm avoidance by moderating susceptibility to affectionless control parenting. Noto K et al. 2021 Brain and behavior
34839083 Oxytocin receptor expression and epigenetic regulation in the anterior cingulate cortex of individuals with a history of severe childhood abuse. Almeida D et al. 2022 Psychoneuroendocrinology
35063684 Oxytocin receptor genotype moderates the association between maternal prenatal stress and infant early self-regulation. Kajanoja J et al. 2022 Psychoneuroendocrinology
35146961 Associations between alcohol use and peripheral, genetic, and epigenetic markers of oxytocin in a general sample of young and older adults. Rung JM et al. 2022 Brain and behavior
35149102 Oxytocin receptor gene (OXTR) polymorphisms and social, emotional and behavioral functioning in children and adolescents: A systematic narrative review. Kohlhoff J et al. 2022 Neuroscience and biobehavioral reviews
35222513 Impact of OXTR Polymorphisms on Subjective Well-Being: The Intermediary Role of Attributional Style. Ji L et al. 2021 Frontiers in genetics
35275212 The OXTR rs53576 impacts moral permissibility of attempted but failed harms in populations of students and prisoners. He L et al. 2022 Social cognitive and affective neuroscience
35314247 Oxytocin receptor genes moderate BDNF epigenetic methylation by childhood trauma. Lee HS et al. 2022 Journal of affective disorders
35462200 Oxytocin modulates sensitivity to acculturation and discrimination stress in pregnancy. Rodriguez ACI et al. 2022 Psychoneuroendocrinology
35564961 The Interaction Effect of Parental Rejection and Oxytocin Receptor Gene Polymorphism on Depression: A Cross-Cultural Study in Non-Clinical Samples. Senese VP et al. 2022 International journal of environmental research and public health
35756198 Gene-Environment Interactions in Face Categorization: Oxytocin Receptor Genotype x Childcare Experience Shortens Reaction Time. Neoh MJY et al. 2022 Frontiers in psychology
35905808 Physical activity associates empathy in Japanese young adults with specific gene variations of oxytocin receptor and vasopressin V1B receptor. Shima T et al. 2022 Physiology & behavior
35995218 Associations of air PM(2.5) level with gut microbiota in Chinese Han preschoolers and effect modification by oxytocin receptor gene polymorphism. Sun Y et al. 2022 Environmental research
36098825 Joint Roles of Oxytocin- and Dopamine-Related Genes and Childhood Parenting Experience in Maternal Supportive Social Network. Koyama Y et al. 2024 Child psychiatry and human development
Help

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.

Software version is: 2.0.1.post761+d5e8e07