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rs1357692

From SNPedia

Orientationplus
Stabilizedplus
Make rs1357692(G;G)
Make rs1357692(G;T)
Make rs1357692(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position107062032
is asnp
is mentioned by
dbSNPrs1357692
ebirs1357692
HLIrs1357692
Exacrs1357692
Varsomers1357692
Maprs1357692
PheGenIrs1357692
hapmaprs1357692
1000 genomesrs1357692
hgdprs1357692
ensemblrs1357692
gopubmedrs1357692
geneviewrs1357692
scholarrs1357692
googlers1357692
pharmgkbrs1357692
gwascentralrs1357692
openSNPrs1357692
23andMers1357692
23andMe allrs1357692
SNP Nexus

SNPshotrs1357692
SNPdbers1357692
MSV3drs1357692
GWAS Ctlgrs1357692
GMAF0.3228
Max Magnitude
? (G;G) (G;T) (T;T) 28
GWAS snp
PMID [PMID 22832961OA-icon.png]
Trait
Title Genome-wide association study of Alzheimer's disease.
Risk Allele
P-val 0.000009
Odds Ratio 1.1600 None