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rs371898076(C;C)

From SNPedia
common in clinvar
Is agenotype
ofrs371898076
GeneMYH7
Chromosome14
Position23,426,833
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(C;C) 0 common in clinvar
(C;T) 6 Familial hypertrophic cardiomyopathy (possible)