RS587783598 DNM2

Health Risk Chr 19:10823886
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What This Variant Does
"CLNSIG=5
Associated Conditions
Centronuclear myopathy
Autosomal dominant centronuclear myopathy
Charcot-Marie-Tooth disease dominant intermediate B
Centronuclear myopathy
Autosomal dominant centronuclear myopathy
Charcot-Marie-Tooth disease dominant intermediate B
Other Variants in DNM2
rs121909088 rs121909089 rs121909090 rs121909091 rs121909092 rs121909093 rs121909094 rs121909095 rs267606772 rs397514735
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