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rs6738962

From SNPedia

Orientationplus
Stabilizedplus
Make rs6738962(A;A)
Make rs6738962(A;G)
Make rs6738962(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position80054047
GeneCTNNA2
is asnp
is mentioned by
dbSNPrs6738962
ebirs6738962
HLIrs6738962
Exacrs6738962
Varsomers6738962
Maprs6738962
PheGenIrs6738962
hapmaprs6738962
1000 genomesrs6738962
hgdprs6738962
ensemblrs6738962
gopubmedrs6738962
geneviewrs6738962
scholarrs6738962
googlers6738962
pharmgkbrs6738962
gwascentralrs6738962
openSNPrs6738962
23andMers6738962
23andMe allrs6738962
SNP Nexus

SNPshotrs6738962
SNPdbers6738962
MSV3drs6738962
GWAS Ctlgrs6738962
GMAF0.07759
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 23535033OA-icon.png]
Trait Alzheimer's disease (cognitive decline)
Title Genome-wide association study of the rate of cognitive decline in Alzheimer's disease.
Risk Allele
P-val 1E-8
Odds Ratio .18 unit decrease