{{Rsnum
|rsid=80356490
|Chromosome=11
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=SLC37A4
|position=119025299
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=SLC37A4
}}{{omim
|id=602671
|rsnum=80356490
|variant=0001
}}{{ClinVar
|rsid=80356490
|Reversed=1
|FwdREF=G
|FwdALT=T
|REF=C
|ALT=A
|RSPOS=118896009
|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.118896009C>A
|CLNSRC=GeneReviews; OMIM Allelic Variant; UniProtKB (variants)
|CLNORIGIN=1
|CLNSRCID=NBK1312; 602671.0001; VAR_003185
|CLNSIG=5
|CLNCUI=C0268146; C0268146
|CLNDBN=Glucose-6-phosphate transport defect; not provided
|Disease=Glucose-6-phosphate transport defect; not provided
|CLNACC=RCV000007330.1; RCV000059116.1
|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 Auto
|PMID=9428641
|Title=Sequence of a putative glucose 6-phosphate translocase, mutated in glycogen storage disease type Ib.
}}

{{PMID Auto
|PMID=10482962
|Title=The putative glucose 6-phosphate translocase gene is mutated in essentially all cases of glycogen storage disease type I non-a.
}}

{{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.
}}

{{PMID Auto
|PMID=11949931
|Title=Type I glycogen storage diseases: disorders of the glucose-6-phosphatase complex.
}}

{{PMID Auto
|PMID=9758626
|Title=A gene on chromosome 11q23 coding for a putative glucose- 6-phosphate translocase is mutated in glycogen-storage disease types Ib and Ic.
|OA=1
}}