rs1061170, CFH

N. diseases: 72
Disease: Low Vision ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Low Vision
CUI: C0042798
Disease: Low Vision
0.010 GeneticVariation BEFREE The common variant in the human complement Factor H gene (CFH), with Tyr402His, is linked to age-related macular degeneration (AMD), a prevalent disorder leading to visual impairment and irreversible blindness in elderly patients. 17399790 2007