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rs35369693

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;G) slight increase in child-onset mood disorder
Make rs35369693(C;C)
Make rs35369693(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position206116696
GeneAVPR1B
is asnp
is mentioned by
dbSNPrs35369693
ebirs35369693
HLIrs35369693
Exacrs35369693
Varsomers35369693
Maprs35369693
PheGenIrs35369693
hapmaprs35369693
1000 genomesrs35369693
hgdprs35369693
ensemblrs35369693
gopubmedrs35369693
geneviewrs35369693
scholarrs35369693
googlers35369693
pharmgkbrs35369693
gwascentralrs35369693
openSNPrs35369693
23andMers35369693
23andMe allrs35369693
SNP Nexus

SNPshotrs35369693
SNPdbers35369693
MSV3drs35369693
GWAS Ctlgrs35369693
GMAF0.02204
Max Magnitude
The very common allele of rs35369693 was observed to be associated with child-onset mood disorders (primarily depression or bipolar disorder) based on transmission disequilibrium testing of 382 Hungarian families. The association is predominantly noticed only in affected females. This SNP represents a variation at amino acid 65 of the AVPR1B gene.[PMID 17909131]