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rs77803164

From SNPedia

Orientationplus
Stabilizedplus
Make rs77803164(A;A)
Make rs77803164(A;G)
Make rs77803164(G;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position138888027
is asnp
is mentioned by
dbSNPrs77803164
ebirs77803164
HLIrs77803164
Exacrs77803164
Varsomers77803164
Maprs77803164
PheGenIrs77803164
hapmaprs77803164
1000 genomesrs77803164
hgdprs77803164
ensemblrs77803164
gopubmedrs77803164
geneviewrs77803164
scholarrs77803164
googlers77803164
pharmgkbrs77803164
gwascentralrs77803164
openSNPrs77803164
23andMers77803164
23andMe allrs77803164
SNP Nexus

SNPshotrs77803164
SNPdbers77803164
MSV3drs77803164
GWAS Ctlgrs77803164
Max Magnitude
GWAS snp
PMID [PMID 24468470]
Trait Cognitive decline (age-related)
Title Genetic susceptibility to accelerated cognitive decline in the US Health and Retirement Study.
Risk Allele
P-val 4E-6
Odds Ratio .02 [0.01279-0.03167] unit decrease