RS759242559 ACTA1
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What This Variant Does
"CLNSIG=5
Associated Conditions
Actin accumulation myopathy
Congenital myopathy 2b
severe infantile
autosomal recessive
ACTA1-related disorder
Alpha-actinopathy
Actin accumulation myopathy
Congenital myopathy 2b
severe infantile
autosomal recessive
ACTA1-related disorder
Alpha-actinopathy
Other Variants in ACTA1