rs41310749
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs41310749(A;A) |
| Make rs41310749(A;G) |
| Make rs41310749(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 3 |
| Position | 38651526 |
| Gene | SCN5A |
| is a | snp |
| is | mentioned by |
| dbSNP | rs41310749 |
| dbSNP (classic) | rs41310749 |
| ClinGen | rs41310749 |
| ebi | rs41310749 |
| HLI | rs41310749 |
| Exac | rs41310749 |
| Gnomad | rs41310749 |
| Varsome | rs41310749 |
| LitVar | rs41310749 |
| Map | rs41310749 |
| PheGenI | rs41310749 |
| Biobank | rs41310749 |
| 1000 genomes | rs41310749 |
| hgdp | rs41310749 |
| ensembl | rs41310749 |
| geneview | rs41310749 |
| scholar | rs41310749 |
| rs41310749 | |
| pharmgkb | rs41310749 |
| gwascentral | rs41310749 |
| openSNP | rs41310749 |
| 23andMe | rs41310749 |
| SNPshot | rs41310749 |
| SNPdbe | rs41310749 |
| MSV3d | rs41310749 |
| GWAS Ctlg | rs41310749 |
| GMAF | 0.14 |
| Max Magnitude | 0 |
[PMID 22370247
] Genetic variants in SCN5A promoter are associated with arrhythmia phenotype severity in patients with heterozygous loss of function mutation
