RS121909521 ACTA1

Health Risk Chr 1:229433067
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What This Variant Does
"[OMIM:?]
Associated Conditions
Congenital myopathy 2b
severe infantile
autosomal recessive
Congenital myopathy 2c
autosomal dominant
Actin accumulation myopathy
Progressive scapulohumeroperoneal distal myopathy
Actin accumulation myopathy
Congenital myopathy 2b
severe infantile
autosomal recessive
Congenital myopathy 2c
autosomal dominant
Actin accumulation myopathy
Progressive scapulohumeroperoneal distal myopathy
Other Variants in ACTA1
rs121909519 rs121909520 rs121909522 rs121909523 rs121909524 rs121909525 rs121909526 rs121909527 rs121909528 rs121909529
Ask Dr. Hemsworth about this variant