RS869025486 MYL3

Health Risk Chr 3:46859505
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What This Variant Does
"CLNSIG=4
Associated Conditions
Primary familial hypertrophic cardiomyopathy
Hypertrophic cardiomyopathy
Primary familial hypertrophic cardiomyopathy
Hypertrophic cardiomyopathy
Other Variants in MYL3
rs104893748 rs199474703 rs199474707 rs199474705 rs199474706 rs202141423 rs145520567 rs147584015 rs727505197 rs148310342
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