{{Rsnum
|rsid=80356492
|Chromosome=11
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=SLC37A4
|Gene_s=SLC37A4
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|position=119025215
}}{{ClinVar
|ALT=T
|CHROM=11
|CLNACC=RCV000020461.1; RCV000059118.1
|CLNALLE=1
|CLNDBN=Glucose-6-phosphate transport defect; not provided
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1312:C0268146:232220:364:79259:30102006
|CLNHGVS=NC_000011.9:g.118895925C>T
|CLNORIGIN=0
|CLNSIG=5
|CLNSRC=GeneReviews; UniProtKB (variants)
|CLNSRCID=NBK1312; VAR_025602
|Disease=Glucose-6-phosphate transport defect; not provided
|FwdALT=A
|FwdREF=G
|GENEINFO=SLC37A4:2542
|GENE_ID=2542
|GENE_NAME=SLC37A4
|REF=C
|RSPOS=118895925
|Reversed=1
|SAO=1
|SSR=0
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050368000000000002110100
|WGT=0
|dbSNPBuildID=131
|rsid=80356492
}}{{PMID Auto
|PMID=10518030
|Title=Mutations in the glucose-6-phosphate transporter (G6PT) gene in patients with glycogen storage diseases type 1b and 1c.
}}

{{PMID Auto
|PMID=10923042
|Title=Molecular analysis in glycogen storage disease 1 non-A: DHPLC detection of the highly prevalent exon 8 mutations of the G6PT1 gene in German patients.
}}