rs9470361
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs9470361(A;A) |
Make rs9470361(A;G) |
Make rs9470361(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 36655602 |
is a | snp |
is | mentioned by |
dbSNP | rs9470361 |
dbSNP (classic) | rs9470361 |
ClinGen | rs9470361 |
ebi | rs9470361 |
HLI | rs9470361 |
Exac | rs9470361 |
Gnomad | rs9470361 |
Varsome | rs9470361 |
LitVar | rs9470361 |
Map | rs9470361 |
PheGenI | rs9470361 |
Biobank | rs9470361 |
1000 genomes | rs9470361 |
hgdp | rs9470361 |
ensembl | rs9470361 |
geneview | rs9470361 |
scholar | rs9470361 |
rs9470361 | |
pharmgkb | rs9470361 |
gwascentral | rs9470361 |
openSNP | rs9470361 |
23andMe | rs9470361 |
SNPshot | rs9470361 |
SNPdbe | rs9470361 |
MSV3d | rs9470361 |
GWAS Ctlg | rs9470361 |
GMAF | 0.2287 |
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 | 3E-27 |
Odds Ratio | 0.8700 [0.71-1.03] ms increase |