RS104894655 TCAP

Health Risk Chr 17:39665762
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What This Variant Does
"[OMIM:?]
Associated Conditions
Autosomal recessive limb-girdle muscular dystrophy type 2G
Hypertrophic cardiomyopathy 25
Primary dilated cardiomyopathy
Primary familial hypertrophic cardiomyopathy
Cardiovascular phenotype
Autosomal recessive limb-girdle muscular dystrophy type 2G
Hypertrophic cardiomyopathy 25
Primary dilated cardiomyopathy
Primary familial hypertrophic cardiomyopathy
Cardiovascular phenotype
Other Variants in TCAP
rs786205076 rs397516861 rs397516862 rs149585781 rs397516863 rs146502276 rs45495192 rs773317399 rs146906267 rs372538567
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