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rs80338777(A;G)

From SNPedia

possibility of Hypokalemic periodic paralysis
Is agenotype
ofrs80338777
GeneCACNA1S
Chromosome1
Position201,077,915
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 rs80338777(A) allele may be at risk for this disorder. However, this variant may well have incomplete penetrance, meaning that individuals will vary widely in the degree to which they are affected.