{{Rsnum
|rsid=137852888
|Chromosome=3
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=GBE1
|position=81577973
|Gene_s=GBE1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=607839
|variant=0006
|rsnum=137852888
}}{{ClinVar
|rsid=137852888
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=81627124
|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.81627124G>A
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NBK5300; 607839.0006
|CLNSIG=5
|CLNCUI=CN068579; CN068580
|CLNDBN=GLYCOGEN STORAGE DISEASE IV, CLASSIC HEPATIC; GLYCOGEN STORAGE DISEASE IV, CHILDHOOD NEUROMUSCULAR; Glycogen storage disease, type IV
|Disease=GLYCOGEN STORAGE DISEASE IV; GLYCOGEN STORAGE DISEASE IV; Glycogen storage disease
|CLNACC=RCV000002913.1; RCV000002914.1; RCV000056093.1
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen; GeneReviews:GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=CN068579; CN068580; NBK115333:NBK5300:C0017923:232500:367:11179002
}}