{{Rsnum
|rsid=137852889
|Chromosome=3
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=GBE1
|position=81537080
|Gene_s=GBE1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=607839
|variant=0010
|rsnum=137852889
}}{{ClinVar
|rsid=137852889
|Reversed=1
|FwdREF=A
|FwdALT=G
|REF=T
|ALT=C
|RSPOS=81586231
|CHROM=3
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=GBE1:2632
|GENE_NAME=GBE1
|GENE_ID=2632
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000003.11:g.81586231T>C
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NBK5300; 607839.0010
|CLNSIG=5
|CLNCUI=CN068582
|CLNDBN=GLYCOGEN STORAGE DISEASE IV, FATAL PERINATAL NEUROMUSCULAR; Glycogen storage disease, type IV
|Disease=GLYCOGEN STORAGE DISEASE IV; Glycogen storage disease
|CLNACC=RCV000002919.1; RCV000056095.1
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen; GeneReviews:GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=CN068582; NBK115333:NBK5300:C0017923:232500:367:11179002
}}