rs80338784(A;G)
From SNPedia
possibility of Hypokalemic periodic paralysis |
Is a | genotype |
of | rs80338784 |
Gene | SCN4A, LOC105371858 |
Chromosome | 17 |
Position | 63,959,278 |
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 rs80338784(A) allele may be at risk for this disorder.