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rs767770

From SNPedia

Orientationplus
Stabilizedplus
Make rs767770(C;C)
Make rs767770(C;T)
Make rs767770(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position121336257
is asnp
is mentioned by
dbSNPrs767770
ebirs767770
HLIrs767770
Exacrs767770
Varsomers767770
Maprs767770
PheGenIrs767770
hapmaprs767770
1000 genomesrs767770
hgdprs767770
ensemblrs767770
gopubmedrs767770
geneviewrs767770
scholarrs767770
googlers767770
pharmgkbrs767770
gwascentralrs767770
openSNPrs767770
23andMers767770
23andMe allrs767770
SNP Nexus

SNPshotrs767770
SNPdbers767770
MSV3drs767770
GWAS Ctlgrs767770
GMAF0.112
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 20889312]
Trait Bipolar disorder and schizophrenia
Title A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.
Risk Allele
P-val 6E-6
Odds Ratio 1.72 [NR]