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rs326946

From SNPedia

Orientationminus
Stabilizedminus
Make rs326946(G;G)
Make rs326946(G;T)
Make rs326946(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position110628530
GeneARHGAP20
is asnp
is mentioned by
dbSNPrs326946
ebirs326946
HLIrs326946
Exacrs326946
Varsomers326946
Maprs326946
PheGenIrs326946
hapmaprs326946
1000 genomesrs326946
hgdprs326946
ensemblrs326946
gopubmedrs326946
geneviewrs326946
scholarrs326946
googlers326946
pharmgkbrs326946
gwascentralrs326946
openSNPrs326946
23andMers326946
23andMe allrs326946
SNP Nexus

SNPshotrs326946
SNPdbers326946
MSV3drs326946
GWAS Ctlgrs326946
GMAF0.2778
Max Magnitude
? (G;G) (G;T) (T;T) 28
GWAS snp
PMID [PMID 23535033OA-icon.png]
Trait Alzheimer's disease (cognitive decline)
Title Genome-wide association study of the rate of cognitive decline in Alzheimer's disease.
Risk Allele
P-val 7E-7
Odds Ratio .16 unit decrease


[PMID 15660291OA-icon.png] Population structure, admixture, and aging-related phenotypes in African American adults: the Cardiovascular Health Study.