{{Rsnum
|rsid=80356485
|Chromosome=17
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=G6PC
|position=42911076
|Gene_s=G6PC
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=80356485
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=41063093
|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.41063093C>T
|CLNSRC=GeneReviews
|CLNORIGIN=0
|CLNSRCID=NBK1312
|CLNSIG=5
|CLNCUI=C0268146
|CLNDBN=Glucose-6-phosphate transport defect
|Disease=Glucose-6-phosphate transport defect
|CLNACC=RCV000020137.1
|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=7573034
|Title=Genetic basis of glycogen storage disease type 1a: prevalent mutations at the glucose-6-phosphatase locus.
|OA=1
}}