rs13165478
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs13165478(A;A) |
Make rs13165478(A;G) |
Make rs13165478(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 5 |
Position | 154489480 |
is a | snp |
is | mentioned by |
dbSNP | rs13165478 |
dbSNP (classic) | rs13165478 |
ClinGen | rs13165478 |
ebi | rs13165478 |
HLI | rs13165478 |
Exac | rs13165478 |
Gnomad | rs13165478 |
Varsome | rs13165478 |
LitVar | rs13165478 |
Map | rs13165478 |
PheGenI | rs13165478 |
Biobank | rs13165478 |
1000 genomes | rs13165478 |
hgdp | rs13165478 |
ensembl | rs13165478 |
geneview | rs13165478 |
scholar | rs13165478 |
rs13165478 | |
pharmgkb | rs13165478 |
gwascentral | rs13165478 |
openSNP | rs13165478 |
23andMe | rs13165478 |
SNPshot | rs13165478 |
SNPdbe | rs13165478 |
MSV3d | rs13165478 |
GWAS Ctlg | rs13165478 |
GMAF | 0.3994 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 21076409![]() |
Trait | |
Title | Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction |
Risk Allele | A |
P-val | 7E-14 |
Odds Ratio | 0.5500 [0.41-0.69] ms decrease |