RS786205076 TCAP

Health Risk Chr 17:39665466
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What This Variant Does
"CLNSIG=5
Associated Conditions
Autosomal recessive limb-girdle muscular dystrophy type 2G
Primary familial hypertrophic cardiomyopathy
Hypertrophic cardiomyopathy 25
Cardiovascular phenotype
Cardiovascular phenotype
Autosomal recessive limb-girdle muscular dystrophy type 2G
Primary familial hypertrophic cardiomyopathy
Hypertrophic cardiomyopathy 25
Cardiovascular phenotype
Cardiovascular phenotype
Other Variants in TCAP
rs104894655 rs397516861 rs397516862 rs149585781 rs397516863 rs146502276 rs45495192 rs773317399 rs146906267 rs372538567
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