RS121909092 DNM2

Health Risk Chr 19:10793829
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What This Variant Does
"[OMIM:?]
Associated Conditions
Autosomal dominant centronuclear myopathy
Centronuclear myopathy
Myopathy
Charcot-Marie-Tooth disease dominant intermediate B
DNM2-related disorder
Autosomal dominant centronuclear myopathy
Centronuclear myopathy
Myopathy
Charcot-Marie-Tooth disease dominant intermediate B
DNM2-related disorder
Other Variants in DNM2
rs121909088 rs121909089 rs121909090 rs121909091 rs121909093 rs121909094 rs121909095 rs267606772 rs397514735 rs144250390
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