RS104894728 TNNI3

Health Risk Chr 19:55151898
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What This Variant Does
"rs104894728, also known as c.569A&gt
Associated Conditions
Cardiomyopathy
familial restrictive
1
Hypertrophic cardiomyopathy 7
Cardiomyopathy
familial restrictive
1
Hypertrophic cardiomyopathy 7
Other Variants in TNNI3
rs104894724 rs104894725 rs104894727 rs104894729 rs104894730 rs121917760 rs121917761 rs267607130 rs267607129 rs267607127
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