Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs3803036
rs3803036
Entrez Id: 5801
Gene Symbol: PTPRR
PTPRR
CUI: C0271183
Disease:
Severe myopia
0.010 GeneticVariation BEFREE Several genetic markers were nominally significantly associated with high-grade myopia in qualitative testing, including rs3803036, a missense mutation in PTPRR (P = 9.1 × 10(-4)) and rs4764971, an intronic SNP in UHRF1BP1L (P = 6.1 × 10(-4)). 23422819 2013