rs3757458
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs3757458(A;A) |
Make rs3757458(A;G) |
Make rs3757458(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 7 |
Position | 101238122 |
Gene | CLDN15 |
is a | snp |
is | mentioned by |
dbSNP | rs3757458 |
dbSNP (classic) | rs3757458 |
ClinGen | rs3757458 |
ebi | rs3757458 |
HLI | rs3757458 |
Exac | rs3757458 |
Gnomad | rs3757458 |
Varsome | rs3757458 |
LitVar | rs3757458 |
Map | rs3757458 |
PheGenI | rs3757458 |
Biobank | rs3757458 |
1000 genomes | rs3757458 |
hgdp | rs3757458 |
ensembl | rs3757458 |
geneview | rs3757458 |
scholar | rs3757458 |
rs3757458 | |
pharmgkb | rs3757458 |
gwascentral | rs3757458 |
openSNP | rs3757458 |
23andMe | rs3757458 |
SNPshot | rs3757458 |
SNPdbe | rs3757458 |
MSV3d | rs3757458 |
GWAS Ctlg | rs3757458 |
GMAF | 0.05051 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 23166209] |
Trait | QT interval |
Title | Impact of Ancestry and Common Genetic Variants on QT Interval in African Americans. |
Risk Allele | A |
P-val | 2E-6 |
Odds Ratio | 8.00 [4.77-11.23] unit decrease |