rs2961024
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs2961024(A;A) |
Make rs2961024(A;C) |
Make rs2961024(C;C) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 7 |
Position | 92061756 |
Gene | AKAP9 |
is a | snp |
is | mentioned by |
dbSNP | rs2961024 |
dbSNP (classic) | rs2961024 |
ClinGen | rs2961024 |
ebi | rs2961024 |
HLI | rs2961024 |
Exac | rs2961024 |
Gnomad | rs2961024 |
Varsome | rs2961024 |
LitVar | rs2961024 |
Map | rs2961024 |
PheGenI | rs2961024 |
Biobank | rs2961024 |
1000 genomes | rs2961024 |
hgdp | rs2961024 |
ensembl | rs2961024 |
geneview | rs2961024 |
scholar | rs2961024 |
rs2961024 | |
pharmgkb | rs2961024 |
gwascentral | rs2961024 |
openSNP | rs2961024 |
23andMe | rs2961024 |
SNPshot | rs2961024 |
SNPdbe | rs2961024 |
MSV3d | rs2961024 |
GWAS Ctlg | rs2961024 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
|
[PMID 25087618] AKAP9 is a genetic modifier of congenital long-QT syndrome type 1