Disease: Oculocerebrorenal Syndrome ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs398123287
rs398123287
Entrez Id: 4952
Gene Symbol: OCRL
OCRL
CUI: C0028860
Disease:
Oculocerebrorenal Syndrome 		0.700 GeneticVariation UNIPROT