Variant: rs119456959 

    present in Gene: NPHP3;NPHP3-ACAD11
    present in Chromosome: 3
    Position on Chromosome: 132682077
    Alleles of this Variant: CCT/-

rs119456959 in NPHP3;NPHP3-ACAD11 gene and Nephronophthisis PMID 12872122 2003 Mutations in a novel gene, NPHP3, cause adolescent nephronophthisis, tapeto-retinal degeneration and hepatic fibrosis.