CTSB, cathepsin B, 1508

N. diseases: 304; N. variants: 17
Disease: Parkinson Disease ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2740594
rs2740594
Entrez Id: 1508
Gene Symbol: CTSB
CTSB
CUI: C0030567
Disease:
Parkinson Disease 		A 0.700 GeneticVariation GWASCAT A meta-analysis of genome-wide association studies identifies 17 new Parkinson's disease risk loci. 28892059 2017