Disease: Oculocerebrorenal Syndrome ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs776743373
rs776743373
Entrez Id: 4952
Gene Symbol: OCRL
OCRL
CUI: C0028860
Disease:
Oculocerebrorenal Syndrome 		A 0.700 CausalMutation CLINVAR