RS2527436292 ACTA1

Health Risk Chr 1:229431848
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Associated Conditions
Congenital myopathy 2c
severe infantile
autosomal dominant
Congenital myopathy 2c
severe infantile
autosomal dominant
Other Variants in ACTA1
rs121909519 rs121909520 rs121909521 rs121909522 rs121909523 rs121909524 rs121909525 rs121909526 rs121909527 rs121909528
Ask Dr. Hemsworth about this variant