Variant: rs1060501915 

    present in Gene: MFN2
    present in Chromosome: 1
    Position on Chromosome: 11998842
    Alleles of this Variant: TGGTGGC/-

rs1060501915 in MFN2 gene and Hereditary Motor and Sensory-Neuropathy Type II PMID 21508331 2011 MFN2 mutations cause severe phenotypes in most patients with CMT2A.