rs80338788(A;G)
From SNPedia
| possibility of Hypokalemic periodic paralysis |
| Is a | genotype |
| of | rs80338788 |
| Gene | SCN4A, LOC105371858 |
| Chromosome | 17 |
| Position | 63,959,269 |
| mentioned | by |
| Magnitude | 3 |
| Repute | Bad |
| Geno | Mag | Summary |
|---|---|---|
| (A;G) | 3 | possibility of Hypokalemic periodic paralysis |
| (G;G) | 0 | common in clinvar |
Hypokalemic periodic paralysis (hypoKPP) is an autosomal dominant skeletal muscle disorder, so carriers of one rs80338788(A) allele may be at risk for this disorder.
