rs9436640
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs9436640(G;G) |
Make rs9436640(G;T) |
Make rs9436640(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 61408005 |
Gene | NFIA |
is a | snp |
is | mentioned by |
dbSNP | rs9436640 |
dbSNP (classic) | rs9436640 |
ClinGen | rs9436640 |
ebi | rs9436640 |
HLI | rs9436640 |
Exac | rs9436640 |
Gnomad | rs9436640 |
Varsome | rs9436640 |
LitVar | rs9436640 |
Map | rs9436640 |
PheGenI | rs9436640 |
Biobank | rs9436640 |
1000 genomes | rs9436640 |
hgdp | rs9436640 |
ensembl | rs9436640 |
geneview | rs9436640 |
scholar | rs9436640 |
rs9436640 | |
pharmgkb | rs9436640 |
gwascentral | rs9436640 |
openSNP | rs9436640 |
23andMe | rs9436640 |
SNPshot | rs9436640 |
SNPdbe | rs9436640 |
MSV3d | rs9436640 |
GWAS Ctlg | rs9436640 |
GMAF | 0.427 |
Max Magnitude | 0 |
? | (G;G) (G;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 21076409] |
Trait | |
Title | Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction |
Risk Allele | G |
P-val | 5E-18 |
Odds Ratio | 0.5900 [0.45-0.73] ms decrease |