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rs104894369(A;G)

From SNPedia

Familial hypertrophic cardiomyopathy (possible)
Is agenotype
ofrs104894369
GeneMYL2
Chromosome12
Position110,914,287
Merged fromRs28933099
mentionedby
Magnitude6
ReputeBad
Geno Mag Summary
(A;G) 6 Familial hypertrophic cardiomyopathy (possible)
(G;G) 0 common in clinvar

see discussion at rs104894369