RS104894727 TNNI3

Health Risk Chr 19:55151881
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What This Variant Does
"rs104894727, also known as c.586G&gt
Associated Conditions
Hypertrophic cardiomyopathy 7
Primary familial hypertrophic cardiomyopathy
Hypertrophic cardiomyopathy
Cardiomyopathy
Dilated cardiomyopathy 1FF
familial restrictive
1
Dilated cardiomyopathy 2A
Cardiovascular phenotype
Hypertrophic cardiomyopathy 7
Primary familial hypertrophic cardiomyopathy
Hypertrophic cardiomyopathy
Cardiomyopathy
Dilated cardiomyopathy 1FF
familial restrictive
Other Variants in TNNI3
rs104894724 rs104894725 rs104894728 rs104894729 rs104894730 rs121917760 rs121917761 rs267607130 rs267607129 rs267607127
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