RS587780271 ACTA1

Health Risk Chr 1:229432597
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What This Variant Does
"CLNSIG=4
Associated Conditions
Nemaline myopathy 3
autosomal dominant or recessive
Nemaline myopathy 3
autosomal dominant or recessive
Other Variants in ACTA1
rs121909519 rs121909520 rs121909521 rs121909522 rs121909523 rs121909524 rs121909525 rs121909526 rs121909527 rs121909528
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