RS121909519 ACTA1

Health Risk Chr 1:229432723
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What This Variant Does
"[OMIM:?]
Associated Conditions
Actin accumulation myopathy
ACTA1-related myopathies
Congenital myopathy 2b
severe infantile
autosomal recessive
Actin accumulation myopathy
ACTA1-related myopathies
Congenital myopathy 2b
severe infantile
autosomal recessive
Other Variants in ACTA1
rs121909520 rs121909521 rs121909522 rs121909523 rs121909524 rs121909525 rs121909526 rs121909527 rs121909528 rs121909529
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