RS786204950 ACTN2

Health Risk Chr 1:236757607
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Cardiomyopathy
familial hypertrophic
23
with or without ventricular noncompaction
Cardiomyopathy
familial hypertrophic
23
with or without ventricular noncompaction
Other Variants in ACTN2
rs121434525 rs193922635 rs1150181 rs397516562 rs397516563 rs139515659 rs376923220 rs200529923 rs200248944 rs142142718
Ask Dr. Hemsworth about this variant