RS148395034 TRIM63

Health Risk Chr 1:26058482
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Associated Conditions
Primary familial hypertrophic cardiomyopathy
Inborn genetic diseases
Hypertrophic cardiomyopathy
Cardiovascular phenotype
Cardiomyopathy
familial hypertrophic
31
Primary familial hypertrophic cardiomyopathy
Inborn genetic diseases
Hypertrophic cardiomyopathy
Cardiovascular phenotype
Cardiomyopathy
familial hypertrophic
31
Other Variants in TRIM63
rs140523053 rs200811483 rs61749355 rs377334933 rs540072010 rs750765152 rs141049472 rs556820261
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