{{Rsnum
|rsid=80338671
|Chromosome=3
|Orientation=plus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=GBE1
|position=81642787
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=GBE1
}}{{omim
|id=607839
|rsnum=80338671
|variant=0002
}}{{ClinVar
|rsid=80338671
|Reversed=1
|FwdREF=A
|FwdALT=C,G
|REF=T
|ALT=C,G
|RSPOS=81691938
|CHROM=3
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050368000000000002110100
|GENEINFO=GBE1:2632
|GENE_NAME=GBE1
|GENE_ID=2632
|WGT=0
|VC=SNV
|CLNALLE=2
|CLNHGVS=NC_000003.11:g.81691938T>G
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=NBK5300; 607839.0002
|CLNSIG=5
|CLNCUI=CN068577; C0017923
|CLNDBN=GLYCOGEN STORAGE DISEASE IV, NONPROGRESSIVE HEPATIC; Adult polyglucosan body disease; Glycogen storage disease, type IV
|Disease=GLYCOGEN STORAGE DISEASE IV; Adult polyglucosan body disease; Glycogen storage disease
|CLNACC=RCV000002907.1; RCV000002908.1; RCV000020163.1
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=MedGen; GeneReviews:GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=CN068577; NBK115333:NBK5300:C0017923:232500:367:11179002
}}{{PMID Auto
|PMID=8613547
|Title=Hepatic and neuromuscular forms of glycogen storage disease type IV caused by mutations in the same glycogen-branching enzyme gene.
|OA=1
}}