Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 5799
Gene Symbol: PTPRN2
PTPRN2
CUI: C0154778
Disease: Myopia, Degenerative
Myopia, Degenerative
0.100 GeneticVariation GWASCAT A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population. 23049088

2012