rs757092
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs757092(A;A) |
Make rs757092(A;G) |
Make rs757092(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 11 |
Position | 2477948 |
Gene | KCNQ1 |
is a | snp |
is | mentioned by |
dbSNP | rs757092 |
dbSNP (classic) | rs757092 |
ClinGen | rs757092 |
ebi | rs757092 |
HLI | rs757092 |
Exac | rs757092 |
Gnomad | rs757092 |
Varsome | rs757092 |
LitVar | rs757092 |
Map | rs757092 |
PheGenI | rs757092 |
Biobank | rs757092 |
1000 genomes | rs757092 |
hgdp | rs757092 |
ensembl | rs757092 |
geneview | rs757092 |
scholar | rs757092 |
rs757092 | |
pharmgkb | rs757092 |
gwascentral | rs757092 |
openSNP | rs757092 |
23andMe | rs757092 |
SNPshot | rs757092 |
SNPdbe | rs757092 |
MSV3d | rs757092 |
GWAS Ctlg | rs757092 |
GMAF | 0.4789 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 19305408] Common variants at ten loci influence QT interval duration in the QTGEN Study.