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rs144662445

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs144662445(A;G)
Make rs144662445(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position92079771
GeneAKAP9
is asnp
is mentioned by
dbSNPrs144662445
ebirs144662445
HLIrs144662445
Exacrs144662445
Varsomers144662445
Maprs144662445
PheGenIrs144662445
hapmaprs144662445
1000 genomesrs144662445
hgdprs144662445
ensemblrs144662445
gopubmedrs144662445
geneviewrs144662445
scholarrs144662445
googlers144662445
pharmgkbrs144662445
gwascentralrs144662445
openSNPrs144662445
23andMers144662445
23andMe allrs144662445
SNP Nexus

SNPshotrs144662445
SNPdbers144662445
MSV3drs144662445
GWAS Ctlgrs144662445
Max Magnitude0

[PMID 25172201OA-icon.png] Two rare AKAP9 variants are associated with Alzheimer's disease in African Americans

ClinVar
Risk rs144662445(G;G)
Alt rs144662445(G;G)
Reference rs144662445(A;A)
Significance Non-pathogenic
Disease not specified
Variation info
Gene AKAP9
CLNDBN not specified
Reversed 0
HGVS NC_000007.13:g.91709085A>G
CLNSRC ClinVar GeneDx
CLNACC RCV000123584.1,