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rs1021769

From SNPedia

Orientationplus
Stabilizedplus
Make rs1021769(C;C)
Make rs1021769(C;T)
Make rs1021769(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position123856740
is asnp
is mentioned by
dbSNPrs1021769
dbSNP (classic)rs1021769
ClinGenrs1021769
ebirs1021769
HLIrs1021769
Exacrs1021769
Gnomadrs1021769
Varsomers1021769
LitVarrs1021769
Maprs1021769
PheGenIrs1021769
Biobankrs1021769
1000 genomesrs1021769
hgdprs1021769
ensemblrs1021769
geneviewrs1021769
scholarrs1021769
googlers1021769
pharmgkbrs1021769
gwascentralrs1021769
openSNPrs1021769
23andMers1021769
SNPshotrs1021769
SNPdbers1021769
MSV3drs1021769
GWAS Ctlgrs1021769
Max Magnitude0
? (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 7E-6
Odds Ratio .02 [0.00853-0.02172] unit decrease