RS587777387 ACTG2

Health Risk Chr 2:73914835
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What This Variant Does
"CLNSIG=5
Associated Conditions
Visceral myopathy 1
Inborn genetic diseases
Chronic intestinal pseudoobstruction
Megacystis
Megacystis-microcolon-intestinal hypoperistalsis syndrome 5
Visceral neuropathy
familial
3
autosomal dominant
Visceral myopathy 1
Inborn genetic diseases
Chronic intestinal pseudoobstruction
Megacystis
Megacystis-microcolon-intestinal hypoperistalsis syndrome 5
Visceral neuropathy
Other Variants in ACTG2
rs757905857 rs1057522054 rs1057520694 rs140943831 rs1553396458 rs1573468797 rs1573461481 rs1573462811 rs1462841170 rs2104815901
Ask Dr. Hemsworth about this variant