Variant: rs587777572 

    present in Gene: PXDN
    present in Chromosome: 2
    Position on Chromosome: 1649142
    Alleles of this Variant: G/A;C

rs587777572 in PXDN gene and ANTERIOR SEGMENT DYSGENESIS 7 PMID 21907015 2011 Homozygous mutations in PXDN cause congenital cataract, corneal opacity, and developmental glaucoma.