RS121909531 ACTA1

Health Risk Chr 1:229431633
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What This Variant Does
"[OMIM:?]
Associated Conditions
Congenital myopathy with fiber type disproportion
Actin accumulation myopathy
Congenital myopathy 2c
severe infantile
autosomal dominant
Alpha-actinopathy
Progressive scapulohumeroperoneal distal myopathy
Congenital myopathy with fiber type disproportion
Actin accumulation myopathy
Congenital myopathy 2c
severe infantile
autosomal dominant
Alpha-actinopathy
Progressive scapulohumeroperoneal distal myopathy
Other Variants in ACTA1
rs121909519 rs121909520 rs121909521 rs121909522 rs121909523 rs121909524 rs121909525 rs121909526 rs121909527 rs121909528
Ask Dr. Hemsworth about this variant