Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Retinal Dystrophies
CUI: C0854723
Disease: Retinal Dystrophies
0.700 GeneticVariation CLINVAR
Nystagmus
CUI: C0028738
Disease: Nystagmus
0.700 GeneticVariation CLINVAR
Cataract
CUI: C0086543
Disease: Cataract
0.700 GeneticVariation CLINVAR
Severe myopia
CUI: C0271183
Disease: Severe myopia
0.700 GeneticVariation CLINVAR