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rs121908555(C;T)

From SNPedia

possibility of Hypokalemic periodic paralysis
Is agenotype
ofrs121908555
GeneSCN4A
Chromosome17
Position63,945,608
mentionedby
Magnitude3
ReputeBad
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.