rs3815459
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs3815459(A;A) |
Make rs3815459(A;G) |
Make rs3815459(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 7 |
Position | 150947306 |
Gene | KCNH2 |
is a | snp |
is | mentioned by |
dbSNP | rs3815459 |
dbSNP (classic) | rs3815459 |
ClinGen | rs3815459 |
ebi | rs3815459 |
HLI | rs3815459 |
Exac | rs3815459 |
Gnomad | rs3815459 |
Varsome | rs3815459 |
LitVar | rs3815459 |
Map | rs3815459 |
PheGenI | rs3815459 |
Biobank | rs3815459 |
1000 genomes | rs3815459 |
hgdp | rs3815459 |
ensembl | rs3815459 |
geneview | rs3815459 |
scholar | rs3815459 |
rs3815459 | |
pharmgkb | rs3815459 |
gwascentral | rs3815459 |
openSNP | rs3815459 |
23andMe | rs3815459 |
SNPshot | rs3815459 |
SNPdbe | rs3815459 |
MSV3d | rs3815459 |
GWAS Ctlg | rs3815459 |
GMAF | 0.4073 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
23andMe blog Influences QT interval
[PMID 19305408] Common variants at ten loci influence QT interval duration in the QTGEN Study.
[PMID 22688145] Clinical response and side effects of metoclopramide: associations with clinical, demographic, and pharmacogenetic parameters