RS104894729 TNNI3

Health Risk Chr 19:55151892
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What This Variant Does
"rs104894729, also known as c.575G&gt
Associated Conditions
Cardiomyopathy
familial restrictive
1
Hypertrophic cardiomyopathy
Restrictive cardiomyopathy
Primary familial hypertrophic cardiomyopathy
Cardiovascular phenotype
SUDDEN INFANT DEATH SYNDROME
Dilated cardiomyopathy 2A
Hypertrophic cardiomyopathy
Hypertrophic cardiomyopathy
Cardiomyopathy
familial restrictive
1
Hypertrophic cardiomyopathy
Other Variants in TNNI3
rs104894724 rs104894725 rs104894727 rs104894728 rs104894730 rs121917760 rs121917761 rs267607130 rs267607129 rs267607127
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