Have questions? Visit https://www.reddit.com/r/SNPedia

rs80338784(A;G)

From SNPedia
possibility of Hypokalemic periodic paralysis
Is agenotype
ofrs80338784
GeneSCN4A, LOC105371858
Chromosome17
Position63,959,278
mentionedby
Magnitude3
ReputeBad
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.