{{Rsnum
|rsid=80356482
|Chromosome=17
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=G6PC
|position=42909418
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=G6PC
}}{{omim
|id=232200
|rsnum=80356482
|variant=0012
}}{{ClinVar
|rsid=80356482
|Reversed=0
|FwdREF=G
|FwdALT=C
|REF=G
|ALT=C
|RSPOS=41061435
|CHROM=17
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050168000000000002110100
|GENEINFO=G6PC:2538
|GENE_NAME=G6PC
|GENE_ID=2538
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000017.10:g.41061435G>C
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=NBK1312; 613742.0012
|CLNSIG=5
|CLNCUI=CN069618; C0268146
|CLNDBN=Glycogen storage disease type 1A; Glucose-6-phosphate transport defect
|Disease=Glycogen storage disease type 1A; Glucose-6-phosphate transport defect
|CLNACC=RCV000012788.1; RCV000020135.1
|Tags=PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet; GeneReviews:MedGen:OMIM:Orphanet:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1312:CN069618:232200:364:79258; NBK1312:C0268146:232220:364:79259:30102006
}}{{PMID Auto
|PMID=8733042
|Title=Mutation analysis in 24 French patients with glycogen storage disease type 1a.
|OA=1
}}

{{PMID Auto
|PMID=10960498
|Title=Glucose-6-phosphatase mutation G188R confers an atypical glycogen storage disease type 1b phenotype.
}}