rs7562790
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs7562790(G;G) |
| Make rs7562790(G;T) |
| Make rs7562790(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 2 |
| Position | 36446412 |
| Gene | CRIM1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7562790 |
| dbSNP (classic) | rs7562790 |
| ClinGen | rs7562790 |
| ebi | rs7562790 |
| HLI | rs7562790 |
| Exac | rs7562790 |
| Gnomad | rs7562790 |
| Varsome | rs7562790 |
| LitVar | rs7562790 |
| Map | rs7562790 |
| PheGenI | rs7562790 |
| Biobank | rs7562790 |
| 1000 genomes | rs7562790 |
| hgdp | rs7562790 |
| ensembl | rs7562790 |
| geneview | rs7562790 |
| scholar | rs7562790 |
| rs7562790 | |
| pharmgkb | rs7562790 |
| gwascentral | rs7562790 |
| openSNP | rs7562790 |
| 23andMe | rs7562790 |
| SNPshot | rs7562790 |
| SNPdbe | rs7562790 |
| MSV3d | rs7562790 |
| GWAS Ctlg | rs7562790 |
| GMAF | 0.472 |
| 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 | 8E-9 |
| Odds Ratio | 0.3900 [0.25-0.53] ms increase |
