rs7626962(G;G)
From SNPedia
| common in clinvar |
| Is a | genotype |
| of | rs7626962 |
| Gene | SCN5A |
| Chromosome | 3 |
| Position | 38,579,416 |
| mentioned | by |
| Magnitude | 0 |
| Repute | Good |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| (G;T) | 2 | Now: Benign? Formerly: increased susceptibility to long QT syndrome |
| (T;T) | 2 | Now: Benign? Formerly: increased susceptibility to long QT syndrome |
