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rs587782962(G;G)

From SNPedia
common in clinvar
Is agenotype
ofrs587782962
GeneMYH7
Chromosome14
Position23,422,267
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(A;G) 6.2 Familial Hypertrophic Cardiomyopathy
(G;G) 0 common in clinvar