RS140208362 DNM2

Health Risk Chr 19:10796149
Upload your DNA to see your genotype for this variant.
Associated Conditions
Charcot-Marie-Tooth disease dominant intermediate B
Autosomal dominant centronuclear myopathy
Inborn genetic diseases
Charcot-Marie-Tooth disease dominant intermediate B
Autosomal dominant centronuclear myopathy
Inborn genetic diseases
Other Variants in DNM2
rs121909088 rs121909089 rs121909090 rs121909091 rs121909092 rs121909093 rs121909094 rs121909095 rs267606772 rs397514735
Ask Dr. Hemsworth about this variant