Variant: rs370130010 

    present in Gene: NCAPH2;SCO2
    present in Chromosome: 22
    Position on Chromosome: 50524078
    Alleles of this Variant: G/A;T

rs370130010 in NCAPH2;SCO2 gene and MYOPIA 6 (disorder) PMID 25525168 2014 Detection of mutations in LRPAP1, CTSH, LEPREL1, ZNF644, SLC39A5, and SCO2 in 298 families with early-onset high myopia by exome sequencing.

PMID 23643385 2013 Mutations in SCO2 are associated with autosomal-dominant high-grade myopia.

PMID 25959673 2015 Cooperation between COA6 and SCO2 in COX2 maturation during cytochrome c oxidase assembly links two mitochondrial cardiomyopathies.