RS149585781 TCAP

Health Risk Chr 17:39666063
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What This Variant Does
"CLNSIG=5
Associated Conditions
Hypertrophic cardiomyopathy 25
Autosomal recessive limb-girdle muscular dystrophy type 2G
Primary familial hypertrophic cardiomyopathy
Cardiovascular phenotype
Hypertrophic cardiomyopathy 25
Autosomal recessive limb-girdle muscular dystrophy type 2G
Primary familial hypertrophic cardiomyopathy
Cardiovascular phenotype
Other Variants in TCAP
rs104894655 rs786205076 rs397516861 rs397516862 rs397516863 rs146502276 rs45495192 rs773317399 rs146906267 rs372538567
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