RS267606772 DNM2

Health Risk Chr 19:10793799
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What This Variant Does
"CLNSIG=5
Associated Conditions
Autosomal dominant Charcot-Marie-Tooth disease type 2M
Charcot-Marie-Tooth disease dominant intermediate B
Autosomal dominant Charcot-Marie-Tooth disease type 2M
Charcot-Marie-Tooth disease dominant intermediate B
Other Variants in DNM2
rs121909088 rs121909089 rs121909090 rs121909091 rs121909092 rs121909093 rs121909094 rs121909095 rs397514735 rs144250390
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