{{Rsnum
|rsid=80356489
|Chromosome=11
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=SLC37A4
|position=119028223
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=SLC37A4
}}{{omim
|id=602671
|rsnum=80356489
|variant=0003
}}{{ClinVar
|rsid=80356489
|Reversed=1
|FwdREF=T
|FwdALT=C
|REF=A
|ALT=G
|RSPOS=118898933
|CHROM=11
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050368000000000002110100
|GENEINFO=SLC37A4:2542
|GENE_NAME=SLC37A4
|GENE_ID=2542
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.118898933A>G
|CLNSRC=GeneReviews; OMIM Allelic Variant; UniProtKB (variants)
|CLNORIGIN=0
|CLNSRCID=NBK1312; 602671.0003; VAR_007850
|CLNSIG=5
|CLNCUI=C0268146; C0268146
|CLNDBN=Glucose-6-phosphate transport defect; not provided
|Disease=Glucose-6-phosphate transport defect; not provided
|CLNACC=RCV000007332.1; RCV000059128.1
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1312:C0268146:232220:364:79259:30102006
}}{{PMID|9675154}} Molecular analysis of glycogen storage disease type Ib: identification of a prevalent mutation among Japanese patients and assignment of a putative glucose-6-phosphate translocase gene to chromosome 11.

{{PMID|10385064}} Case report: Hepatocellular carcinoma in type 1a glycogen storage disease with identification of a glucose-6-phosphatase gene mutation in one family.

{{PMID|10482875}} Glycogen storage disease type Ib: structural and mutational analysis of the microsomal glucose-6-phosphate transporter gene.

{{PMID|12373566}} Glycogen storage disease type I: diagnosis and phenotype/genotype correlation.

{{PMID|15059622}} Genetic testing of glycogen storage disease type Ib in Japan: five novel G6PT1 mutations and a rapid detection method for a prevalent mutation W118R.

{{PMID|9675154}} Molecular analysis of glycogen storage disease type Ib: identification of a prevalent mutation among Japanese patients and assignment of a putative glucose-6-phosphate translocase gene to chromosome 11.