RS199476312 TPM1

Health Risk Chr 15:63060891
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What This Variant Does
"CLNSIG=1
Associated Conditions
Primary familial hypertrophic cardiomyopathy
Hypertrophic cardiomyopathy
Cardiovascular phenotype
Primary familial hypertrophic cardiomyopathy
Hypertrophic cardiomyopathy
Cardiovascular phenotype
Other Variants in TPM1
rs104894502 rs104894503 rs104894504 rs104894505 rs199476305 rs199476306 rs199476315 rs199476316 rs199476317 rs199476310
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