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rs80338779(G;T)

From SNPedia

possibility of Hypokalemic periodic paralysis
Is agenotype
ofrs80338779
GeneCACNA1S
Chromosome1
Position201,066,283
mentionedby
Magnitude3
ReputeBad
Geno Mag Summary
(G;G) 0 common in clinvar
(G;T) 3 possibility of Hypokalemic periodic paralysis

Hypokalemic periodic paralysis (hypoKPP) is an autosomal dominant skeletal muscle disorder, so carriers of one rs80338779(T) allele may be at risk for this disorder.