RS773159585 MFN2
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Charcot-Marie-Tooth disease type 2A2
Peripheral axonal neuropathy
Distal muscle weakness
Distal lower limb amyotrophy
Charcot-Marie-Tooth disease type 2
Charcot-Marie-Tooth disease
Autosomal dominant and autosomal recessive MFN2-related disorders
Charcot-Marie-Tooth disease type 2A2
Peripheral axonal neuropathy
Distal muscle weakness
Distal lower limb amyotrophy
Charcot-Marie-Tooth disease type 2
Charcot-Marie-Tooth disease
Autosomal dominant and autosomal recessive MFN2-related disorders
Other Variants in MFN2