rs991014
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs991014(A;A) |
| Make rs991014(A;G) |
| Make rs991014(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 18 |
| Position | 44859921 |
| Gene | SETBP1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs991014 |
| dbSNP (classic) | rs991014 |
| ClinGen | rs991014 |
| ebi | rs991014 |
| HLI | rs991014 |
| Exac | rs991014 |
| Gnomad | rs991014 |
| Varsome | rs991014 |
| LitVar | rs991014 |
| Map | rs991014 |
| PheGenI | rs991014 |
| Biobank | rs991014 |
| 1000 genomes | rs991014 |
| hgdp | rs991014 |
| ensembl | rs991014 |
| geneview | rs991014 |
| scholar | rs991014 |
| rs991014 | |
| pharmgkb | rs991014 |
| gwascentral | rs991014 |
| openSNP | rs991014 |
| 23andMe | rs991014 |
| SNPshot | rs991014 |
| SNPdbe | rs991014 |
| MSV3d | rs991014 |
| GWAS Ctlg | rs991014 |
| GMAF | 0.3297 |
| 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 | T |
| P-val | 6E-10 |
| Odds Ratio | 0.4200 [0.28-0.56] ms increase |
