{{Rsnum
|rsid=80356484
|Chromosome=17
|Orientation=plus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=G6PC
|position=42911000
|Gene_s=G6PC
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=80356484
|Reversed=0
|FwdREF=G
|FwdALT=T
|REF=G
|ALT=T
|RSPOS=41063017
|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.41063017G>T
|CLNSRC=GeneReviews
|CLNORIGIN=0
|CLNSRCID=NBK1312
|CLNSIG=5
|CLNCUI=C0268146
|CLNDBN=Glucose-6-phosphate transport defect
|Disease=Glucose-6-phosphate transport defect
|CLNACC=RCV000020136.1
|Tags=PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1312:C0268146:232220:364:79259:30102006
}}{{PMID Auto
|PMID=9630072
|Title=Glucose-6-phosphatase gene (727G-->T) splicing mutation is prevalent in Hong Kong Chinese patients with glycogen storage disease type 1a.
}}