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rs17339677

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs17339677(A;A)
Make rs17339677(A;G)
ReferenceGRCh38 38.1/141
Chromosome20
Position3072433
GeneLOC101929098, OXT
is asnp
is mentioned by
dbSNPrs17339677
ebirs17339677
HLIrs17339677
Exacrs17339677
Varsomers17339677
Maprs17339677
PheGenIrs17339677
hapmaprs17339677
1000 genomesrs17339677
hgdprs17339677
ensemblrs17339677
gopubmedrs17339677
geneviewrs17339677
scholarrs17339677
googlers17339677
pharmgkbrs17339677
gwascentralrs17339677
openSNPrs17339677
23andMers17339677
23andMe allrs17339677
SNP Nexus

SNPshotrs17339677
SNPdbers17339677
MSV3drs17339677
GWAS Ctlgrs17339677
Max Magnitude0
? (A;A) (A;G) (G;G) 28

[PMID 19473710] Mutation analysis of oxytocin gene in individuals with adult separation anxiety

[PMID 18566739OA-icon.png] Variation of the oxytocin/neurophysin I (OXT) gene in four human populations.