rs121908555(C;T)
From SNPedia
| possibility of Hypokalemic periodic paralysis |
| Is a | genotype |
| of | rs121908555 |
| Gene | SCN4A |
| Chromosome | 17 |
| Position | 63,945,608 |
| mentioned | by |
| Magnitude | 3 |
| Repute | Bad |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| (C;T) | 3 | possibility of Hypokalemic periodic paralysis |
Hypokalemic periodic paralysis (hypoKPP) is an autosomal dominant skeletal muscle disorder, so carriers of one rs121908555(T) allele may be at risk for this disorder.
