CSTB, cystatin B, 1476

N. diseases: 155; N. variants: 14
Disease: Epilepsy, Rolandic ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs74315442
rs74315442
Entrez Id: 1476
Gene Symbol: CSTB
CSTB
CUI: C0376532
Disease:
Epilepsy, Rolandic 		A 0.700 CausalMutation CLINVAR Exome-wide analysis of mutational burden in patients with typical and atypical Rolandic epilepsy. 29358611 2018