rs10033900, CFI

N. diseases: 4
Source: ALL
Disease Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0027092
Disease: Myopia
0.010 GeneticVariation BEFREE One SNP (rs10033900) in the CFI gene, which encodes a protein involved in the inflammatory pathway, was significantly associated with myopic CNV in multivariate analysis after correction for multiple testing. 22678500 2012