RS587777386 ACTG2
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What This Variant Does
"CLNSIG=5
Associated Conditions
Visceral myopathy 1
Visceral neuropathy
familial
3
autosomal dominant
Chronic intestinal pseudoobstruction
Megacystis-microcolon-intestinal hypoperistalsis syndrome 5
Constipation
Visceral myopathy 1
Visceral neuropathy
familial
3
autosomal dominant
Chronic intestinal pseudoobstruction
Megacystis-microcolon-intestinal hypoperistalsis syndrome 5
Other Variants in ACTG2