rs9912468
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs9912468(C;C) |
| Make rs9912468(C;G) |
| Make rs9912468(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 17 |
| Position | 66322239 |
| Gene | PRKCA |
| is a | snp |
| is | mentioned by |
| dbSNP | rs9912468 |
| dbSNP (classic) | rs9912468 |
| ClinGen | rs9912468 |
| ebi | rs9912468 |
| HLI | rs9912468 |
| Exac | rs9912468 |
| Gnomad | rs9912468 |
| Varsome | rs9912468 |
| LitVar | rs9912468 |
| Map | rs9912468 |
| PheGenI | rs9912468 |
| Biobank | rs9912468 |
| 1000 genomes | rs9912468 |
| hgdp | rs9912468 |
| ensembl | rs9912468 |
| geneview | rs9912468 |
| scholar | rs9912468 |
| rs9912468 | |
| pharmgkb | rs9912468 |
| gwascentral | rs9912468 |
| openSNP | rs9912468 |
| 23andMe | rs9912468 |
| SNPshot | rs9912468 |
| SNPdbe | rs9912468 |
| MSV3d | rs9912468 |
| GWAS Ctlg | rs9912468 |
| GMAF | 0.4123 |
| Max Magnitude | 0 |
| ? | (C;C) (C;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 | G |
| P-val | 1E-8 |
| Odds Ratio | 0.3900 [0.25-0.53] ms increase |
