CHM, CHM Rab escort protein, 1121

N. diseases: 82; N. variants: 19
Disease: Retinal Dystrophies ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1555955061
rs1555955061
Entrez Id: 1121
Gene Symbol: CHM
CHM
CUI: C0854723
Disease:
Retinal Dystrophies 		C 0.700 GeneticVariation CLINVAR