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rs9980664

From SNPedia

Orientationplus
Stabilizedplus
Make rs9980664(A;A)
Make rs9980664(A;C)
Make rs9980664(C;C)
ReferenceGRCh38 38.1/141
Chromosome21
Position33362204
is asnp
is mentioned by
dbSNPrs9980664
ebirs9980664
HLIrs9980664
Exacrs9980664
Varsomers9980664
Maprs9980664
PheGenIrs9980664
hapmaprs9980664
1000 genomesrs9980664
hgdprs9980664
ensemblrs9980664
gopubmedrs9980664
geneviewrs9980664
scholarrs9980664
googlers9980664
pharmgkbrs9980664
gwascentralrs9980664
openSNPrs9980664
23andMers9980664
23andMe allrs9980664
SNP Nexus

SNPshotrs9980664
SNPdbers9980664
MSV3drs9980664
GWAS Ctlgrs9980664
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 3E-6
Odds Ratio .03 [0.01569-0.03866] unit increase