RS398122936 ACTA1

Health Risk Chr 1:229431727
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Congenital myopathy 2c
severe infantile
autosomal dominant
Congenital myopathy 2c
severe infantile
autosomal dominant
Other Variants in ACTA1
rs121909519 rs121909520 rs121909521 rs121909522 rs121909523 rs121909524 rs121909525 rs121909526 rs121909527 rs121909528
Ask Dr. Hemsworth about this variant