RS121909523 ACTA1

Health Risk Chr 1:229432020
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What This Variant Does
"[OMIM:?]
Associated Conditions
Actin accumulation myopathy
ACTA1-related myopathies
Congenital myopathy with fiber type disproportion
Progressive scapulohumeroperoneal distal myopathy
Congenital myopathy 2b
severe infantile
autosomal recessive
Actin accumulation myopathy
ACTA1-related myopathies
Congenital myopathy with fiber type disproportion
Progressive scapulohumeroperoneal distal myopathy
Congenital myopathy 2b
severe infantile
autosomal recessive
Other Variants in ACTA1
rs121909519 rs121909520 rs121909521 rs121909522 rs121909524 rs121909525 rs121909526 rs121909527 rs121909528 rs121909529
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