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rs10497985

From SNPedia

Orientationplus
Stabilizedplus
Make rs10497985(C;C)
Make rs10497985(C;T)
Make rs10497985(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position212744528
is asnp
is mentioned by
dbSNPrs10497985
ebirs10497985
HLIrs10497985
Exacrs10497985
Varsomers10497985
Maprs10497985
PheGenIrs10497985
hapmaprs10497985
1000 genomesrs10497985
hgdprs10497985
ensemblrs10497985
gopubmedrs10497985
geneviewrs10497985
scholarrs10497985
googlers10497985
pharmgkbrs10497985
gwascentralrs10497985
openSNPrs10497985
23andMers10497985
23andMe allrs10497985
SNP Nexus

SNPshotrs10497985
SNPdbers10497985
MSV3drs10497985
GWAS Ctlgrs10497985
Max Magnitude
? (C;C) (C;T) (T;T) 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 4E-6
Odds Ratio .02 [.009684-0.02406] unit increase