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rs895767

From SNPedia

Orientationplus
Stabilizedplus
Make rs895767(A;A)
Make rs895767(A;C)
Make rs895767(C;C)
ReferenceGRCh38 38.1/141
Chromosome2
Position223158578
is asnp
is mentioned by
dbSNPrs895767
ebirs895767
HLIrs895767
Exacrs895767
Varsomers895767
Maprs895767
PheGenIrs895767
hapmaprs895767
1000 genomesrs895767
hgdprs895767
ensemblrs895767
gopubmedrs895767
geneviewrs895767
scholarrs895767
googlers895767
pharmgkbrs895767
gwascentralrs895767
openSNPrs895767
23andMers895767
23andMe allrs895767
SNP Nexus

SNPshotrs895767
SNPdbers895767
MSV3drs895767
GWAS Ctlgrs895767
Max Magnitude
? (A;A) (A;C) (C;C) 28
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 7E-6
Odds Ratio .01 [0.00572-0.01457] unit decrease