Source: BEFREE

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs4764971
rs4764971
ACTR6 ; DEPDC4
CUI: C0271183
Disease: Severe myopia
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