CSTB, cystatin B, 1476

N. diseases: 155; N. variants: 14
Disease: Unverricht-Lundborg Syndrome ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs386833439
rs386833439
Entrez Id: 1476
Gene Symbol: CSTB
CSTB
CUI: C0751785
Disease:
Unverricht-Lundborg Syndrome 		T 0.700 GeneticVariation CLINVAR
dbSNP: rs386833439
rs386833439
Entrez Id: 1476
Gene Symbol: CSTB
CSTB
CUI: C0751785
Disease:
Unverricht-Lundborg Syndrome 		T 0.700 CausalMutation CLINVAR