Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs587777625
rs587777625
0.800 GeneticVariation UNIPROT SLC39A5 mutations interfering with the BMP/TGF-β pathway in non-syndromic high myopia. 24891338

2014

dbSNP: rs587777625
rs587777625
0.800 GeneticVariation UNIPROT Detection of mutations in LRPAP1, CTSH, LEPREL1, ZNF644, SLC39A5, and SCO2 in 298 families with early-onset high myopia by exome sequencing. 25525168

2014