rs4725982
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs4725982(C;C) |
| Make rs4725982(C;T) |
| Make rs4725982(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 7 |
| Position | 150940775 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4725982 |
| dbSNP (classic) | rs4725982 |
| ClinGen | rs4725982 |
| ebi | rs4725982 |
| HLI | rs4725982 |
| Exac | rs4725982 |
| Gnomad | rs4725982 |
| Varsome | rs4725982 |
| LitVar | rs4725982 |
| Map | rs4725982 |
| PheGenI | rs4725982 |
| Biobank | rs4725982 |
| 1000 genomes | rs4725982 |
| hgdp | rs4725982 |
| ensembl | rs4725982 |
| geneview | rs4725982 |
| scholar | rs4725982 |
| rs4725982 | |
| pharmgkb | rs4725982 |
| gwascentral | rs4725982 |
| openSNP | rs4725982 |
| 23andMe | rs4725982 |
| SNPshot | rs4725982 |
| SNPdbe | rs4725982 |
| MSV3d | rs4725982 |
| GWAS Ctlg | rs4725982 |
| GMAF | 0.3682 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
23andMe blog Influences QT interval
| GWAS snp | |
|---|---|
| PMID | [PMID 19305408 ]
|
| Trait | QT interval |
| Title | Common variants at ten loci influence QT interval duation in the QTGEN Study |
| Risk Allele | T |
| P-val | 5E-16 |
| Odds Ratio | 1.58 [1.23-1.92] msec increase |
| GWAS snp | |
|---|---|
| PMID | [PMID 20062061] |
| Trait | Electrocardiographic traits |
| Title | Genetic variation in SCN10A influences cardiac conduction |
| Risk Allele | A |
| P-val | 0.000003 |
| Odds Ratio | 2.08 [1.20-2.96] ms increase |
[PMID 26600494] Analysis of SNP (single nucleotide polymorphism) multiplex markers related to sudden cardiac death in Brazilian families
