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rs121913626(C;G)

From SNPedia

familial hypertrophic cardiomyopathy mutation
Is agenotype
ofrs121913626
GeneMYH7
Chromosome14
Position23,427,723
mentionedby
Magnitude6
ReputeBad
Geno Mag Summary
(C;G) 6 familial hypertrophic cardiomyopathy mutation
(G;G) 0 common in clinvar

see discussion at rs121913626