RS1179926739 MYOD1

Health Risk Chr 11:17720334
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Associated Conditions
Arthrogryposis multiplex congenita
Autosomal dominant centronuclear myopathy
Myopathy
congenital
with diaphragmatic defects
respiratory insufficiency
and dysmorphic facies
Arthrogryposis multiplex congenita
Autosomal dominant centronuclear myopathy
Myopathy
congenital
with diaphragmatic defects
respiratory insufficiency
and dysmorphic facies
Other Variants in MYOD1
rs147517396 rs768652299
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