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rs80338785(A;C)

From SNPedia

possibility of Hypokalemic periodic paralysis
Is agenotype
ofrs80338785
GeneSCN4A
Chromosome17
Position63,959,270
mentionedby
Magnitude3
ReputeBad
Geno Mag Summary
(A;C) 3 possibility of Hypokalemic periodic paralysis
(C;C) 0 common in complete genomics

Hypokalemic periodic paralysis (hypoKPP) is an autosomal dominant skeletal muscle disorder, so carriers of one rs80338785(A) allele may be at risk for this disorder.