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rs397515963(-;G)

From SNPedia
familial hypertrophic cardiomyopathy mutation
Is agenotype
ofrs397515963
GeneMYBPC3
Chromosome11
Position47,337,729
Merged fromRs796596743
mentionedby
Magnitude7
ReputeBad
Geno Mag Summary
(-;-) 0 common in clinvar
(-;G) 7 familial hypertrophic cardiomyopathy mutation
(G;G) 8 Likely severe cardiomyopathy

see discussion at rs397515963