rs397508118(GCTGC;GCTGC)
From SNPedia
| common in clinvar |
| Is a | genotype |
| of | rs397508118 |
| Gene | KCNQ1 |
| Chromosome | 11 |
| Position | 2,570,723 |
| Merged from | Rs606231414 |
| mentioned | by |
| Magnitude | 0 |
| Repute | Good |
| Geno | Mag | Summary |
|---|---|---|
| (-;GCGCT) | 5 | Romano-Ward Long QT Syndrome |
| (GCGCT;GCGCT) | 0 | common in clinvar |
| (GCTGC;GCTGC) | 0 | common in clinvar |
| (I;I) | 0 | common genotype |
