Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1052020291
rs1052020291
CTSB
0.010 GeneticVariation BEFREE The NS2/C113S mutation also impaired infectious-HCV</span> assembly, DRM localization of NS2 and E2, and colocalization of NS2 with Core and endoplasmic reticulum lipid raft-associated protein 2 (Erlin-2). 31597774

2019