Variant: rs773243225 

    present in Gene: LRPAP1
    present in Chromosome: 4
    Position on Chromosome: 3532232
    Alleles of this Variant: G/A

rs773243225 in LRPAP1 gene and Rare isolated myopia PMID 26271838 2016 Clinical Characterization of LRPAP1-Related Pediatric High Myopia.

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 23830514 2013 Mutations in LRPAP1 are associated with severe myopia in humans.