RS121909089 DNM2
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What This Variant Does
"[OMIM:?]
Associated Conditions
Autosomal dominant centronuclear myopathy
Centronuclear myopathy
Charcot-Marie-Tooth disease dominant intermediate B
Charcot-Marie-Tooth disease dominant intermediate B
Autosomal dominant centronuclear myopathy
Centronuclear myopathy
Charcot-Marie-Tooth disease dominant intermediate B
Charcot-Marie-Tooth disease dominant intermediate B
Other Variants in DNM2