rs144662445
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs144662445(A;G) |
Make rs144662445(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 7 |
Position | 92079771 |
Gene | AKAP9 |
is a | snp |
is | mentioned by |
dbSNP | rs144662445 |
dbSNP (classic) | rs144662445 |
ClinGen | rs144662445 |
ebi | rs144662445 |
HLI | rs144662445 |
Exac | rs144662445 |
Gnomad | rs144662445 |
Varsome | rs144662445 |
LitVar | rs144662445 |
Map | rs144662445 |
PheGenI | rs144662445 |
Biobank | rs144662445 |
1000 genomes | rs144662445 |
hgdp | rs144662445 |
ensembl | rs144662445 |
geneview | rs144662445 |
scholar | rs144662445 |
rs144662445 | |
pharmgkb | rs144662445 |
gwascentral | rs144662445 |
openSNP | rs144662445 |
23andMe | rs144662445 |
SNPshot | rs144662445 |
SNPdbe | rs144662445 |
MSV3d | rs144662445 |
GWAS Ctlg | rs144662445 |
Max Magnitude | 0 |
[PMID 25172201] 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, |