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

rs28930069(C;G)

From SNPedia

Hypokalemic periodic paralysis risk
Is agenotype
ofrs28930069
GeneCACNA1S
Chromosome1
Position201,053,539
mentionedby
Magnitude3.5
ReputeBad
Geno Mag Summary
(C;C) 0 common in clinvar
(C;G) 3.5 Hypokalemic periodic paralysis risk
(G;G) 5 Hypokalemic periodic paralysis risk

Hypokalemic periodic paralysis (hypoKPP) is an autosomal dominant skeletal muscle disorder, so carriers of one rs28930069(G) allele may be at risk for this disorder.