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rs863225269

From SNPedia

ClinVar
Risk rs863225269(C;C)
Alt rs863225269(C;C)
Reference rs863225269(;)
Significance Pathogenic
Disease Familial hypertrophic cardiomyopathy 1
Variation info
Gene MYH6
CLNDBN Familial hypertrophic cardiomyopathy 1
Reversed 1
HGVS NC_000014.8:g.23862180dupG
CLNSRC
CLNACC RCV000201905.1,