{{Rsnum
|rsid=386833441
|Chromosome=21
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=CSTB
|position=43774332
|Gene_s=CSTB
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=C
|CHROM=21
|CLNACC=RCV000049368.1
|CLNALLE=1
|CLNDBN=Unverricht-Lundborg syndrome
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1142:C0751785:254800:308:230423006
|CLNHGVS=NC_000021.8:g.45194213T>C
|CLNSIG=4
|Disease=Unverricht-Lundborg syndrome
|FwdALT=G
|FwdREF=A
|REF=T
|RSPOS=45194213
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;PMC;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050068000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=386833441
|GENEINFO=CSTB:1476
|GENE_ID=1476
|GENE_NAME=CSTB
}}{{PMID Auto
|PMID=9012407
|Title=Identification of mutations in cystatin B, the gene responsible for the Unverricht-Lundborg type of progressive myoclonus epilepsy (EPM1).
|OA=1
}}