Disease: Cortical visual impairment ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1553770577
rs1553770577
Entrez Id: 79876;100532724
Gene Symbol: UBA5;NPHP3-ACAD11
UBA5;NPHP3-ACAD11
CUI: C4048268
Disease:
Cortical visual impairment 		C 0.700 GeneticVariation CLINVAR