rs11772585
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs11772585(C;C) |
Make rs11772585(C;T) |
Make rs11772585(T;T) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 7 |
Position | 91952189 |
Gene | AKAP9 |
is a | snp |
is | mentioned by |
dbSNP | rs11772585 |
dbSNP (classic) | rs11772585 |
ClinGen | rs11772585 |
ebi | rs11772585 |
HLI | rs11772585 |
Exac | rs11772585 |
Gnomad | rs11772585 |
Varsome | rs11772585 |
LitVar | rs11772585 |
Map | rs11772585 |
PheGenI | rs11772585 |
Biobank | rs11772585 |
1000 genomes | rs11772585 |
hgdp | rs11772585 |
ensembl | rs11772585 |
geneview | rs11772585 |
scholar | rs11772585 |
rs11772585 | |
pharmgkb | rs11772585 |
gwascentral | rs11772585 |
openSNP | rs11772585 |
23andMe | rs11772585 |
SNPshot | rs11772585 |
SNPdbe | rs11772585 |
MSV3d | rs11772585 |
GWAS Ctlg | rs11772585 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 25087618] AKAP9 is a genetic modifier of congenital long-QT syndrome type 1