Variant: rs587777276 

    present in Gene: NR2F1
    present in Chromosome: 5
    Position on Chromosome: 93588208
    Alleles of this Variant: T/C

rs587777276 in NR2F1 gene and Optic atrophy, intellectual disability syndrome PMID 24462372 2014 NR2F1 mutations cause optic atrophy with intellectual disability.