RS869025431 FHL1

Health Risk Chr X:136209946
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What This Variant Does
"CLNSIG=4
Associated Conditions
Primary familial hypertrophic cardiomyopathy
X-linked myopathy with postural muscle atrophy
Cardiovascular phenotype
Primary familial hypertrophic cardiomyopathy
X-linked myopathy with postural muscle atrophy
Cardiovascular phenotype
Other Variants in FHL1
rs122458140 rs122458141 rs1603271580 rs122458142 rs122458143 rs122458144 rs122458145 rs122459146 rs122459147 rs122459148
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