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rs80338788(G;G)

From SNPedia

common in clinvar
Is agenotype
ofrs80338788
GeneSCN4A
Chromosome17
Position63,959,269
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(A;G) 3 possibility of Hypokalemic periodic paralysis
(G;G) 0 common in clinvar