RS121909095 DNM2

Health Risk Chr 19:10823862
Upload your DNA to see your genotype for this variant.
What This Variant Does
"[OMIM:?]
Associated Conditions
Severe X-linked myotubular myopathy
Centronuclear myopathy
Charcot-Marie-Tooth disease dominant intermediate B
Autosomal dominant centronuclear myopathy
Fetal akinesia-cerebral and retinal hemorrhage syndrome
Severe X-linked myotubular myopathy
Charcot-Marie-Tooth disease dominant intermediate B
Severe X-linked myotubular myopathy
Centronuclear myopathy
Charcot-Marie-Tooth disease dominant intermediate B
Autosomal dominant centronuclear myopathy
Fetal akinesia-cerebral and retinal hemorrhage syndrome
Severe X-linked myotubular myopathy
Charcot-Marie-Tooth disease dominant intermediate B
Other Variants in DNM2
rs121909088 rs121909089 rs121909090 rs121909091 rs121909092 rs121909093 rs121909094 rs267606772 rs397514735 rs144250390
Ask Dr. Hemsworth about this variant