RS121909522 ACTA1
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What This Variant Does
"[OMIM:?]
Associated Conditions
Actin accumulation myopathy
Congenital myopathy 2c
severe infantile
autosomal dominant
Actin accumulation myopathy
Alpha-actinopathy
Progressive scapulohumeroperoneal distal myopathy
Actin accumulation myopathy
Congenital myopathy 2c
severe infantile
autosomal dominant
Actin accumulation myopathy
Alpha-actinopathy
Progressive scapulohumeroperoneal distal myopathy
Other Variants in ACTA1