RS141019458 TCAP

Health Risk Chr 17:39665425
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What This Variant Does
"CLNSIG=4
Associated Conditions
Hypertrophic cardiomyopathy 25
Primary familial hypertrophic cardiomyopathy
Cardiovascular phenotype
Autosomal recessive limb-girdle muscular dystrophy type 2G
Hypertrophic cardiomyopathy 25
Primary familial hypertrophic cardiomyopathy
Cardiovascular phenotype
Autosomal recessive limb-girdle muscular dystrophy type 2G
Other Variants in TCAP
rs104894655 rs786205076 rs397516861 rs397516862 rs149585781 rs397516863 rs146502276 rs45495192 rs773317399 rs146906267
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