RS768144106 ACTA1

Health Risk Chr 1:229432426
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What This Variant Does
"CLNSIG=4
Associated Conditions
Congenital muscular dystrophy with rigid spine
Congenital myopathy 2b
severe infantile
autosomal recessive
Actin accumulation myopathy
Congenital muscular dystrophy with rigid spine
Congenital myopathy 2b
severe infantile
autosomal recessive
Actin accumulation myopathy
Other Variants in ACTA1
rs121909519 rs121909520 rs121909521 rs121909522 rs121909523 rs121909524 rs121909525 rs121909526 rs121909527 rs121909528
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