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rs3764640

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs3764640(G;T)
Make rs3764640(T;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position1207239
GeneSTK11
is asnp
is mentioned by
dbSNPrs3764640
dbSNP (classic)rs3764640
ClinGenrs3764640
ebirs3764640
HLIrs3764640
Exacrs3764640
Gnomadrs3764640
Varsomers3764640
LitVarrs3764640
Maprs3764640
PheGenIrs3764640
Biobankrs3764640
1000 genomesrs3764640
hgdprs3764640
ensemblrs3764640
geneviewrs3764640
scholarrs3764640
googlers3764640
pharmgkbrs3764640
gwascentralrs3764640
openSNPrs3764640
23andMers3764640
SNPshotrs3764640
SNPdbers3764640
MSV3drs3764640
GWAS Ctlgrs3764640
GMAF0.359
Max Magnitude0
? (G;G) (G;T) (T;T) 28


GWAS snp
PMID [PMID 22005930OA-icon.png]
Trait
Title Genome-wide association study of Alzheimer's disease with psychotic symptoms.
Risk Allele
P-val 0.000008
Odds Ratio 1.4700 None


ClinVar
Risk rs3764640(T;T)
Alt rs3764640(T;T)
Reference Rs3764640(G;G)
Significance Non-pathogenic
Disease not specified
Variation info
Gene STK11
CLNDBN not specified
Reversed 0
HGVS NC_000019.9:g.1207238G>T
CLNSRC
CLNACC RCV000254173.1,