{{Rsnum
|rsid=80359828
|Chromosome=1
|Orientation=minus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=SLC2A1
|position=42927173
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=SLC2A1
}}{{omim
|id=138140
|rsnum=80359828
|variant=0003
}}{{ClinVar
|rsid=80359828
|Reversed=1
|FwdREF=C
|FwdALT=A
|REF=G
|ALT=T
|RSPOS=42927173
|CHROM=1
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050168000605000002110100
|GENEINFO=SLC2A1:6513
|GENE_NAME=SLC2A1
|GENE_ID=6513
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.42927173G>T
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_006516.2:c.1347C>A; 138140.0003
|CLNSIG=5
|CLNCUI=C1847501
|CLNDBN=Glucose transporter type 1 deficiency syndrome
|Disease=Glucose transporter type 1 deficiency syndrome
|CLNACC=RCV000017487.26
|Tags=RV;PM;PMC;SLO;NSN;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1430:C1847501:606777:ORPHA71277
}}{{PMID Auto
|PMID=9462754
|Title=GLUT-1 deficiency syndrome caused by haploinsufficiency of the blood-brain barrier hexose carrier.
}}

{{PMID Auto
|PMID=15622525
|Title=Glut-1 deficiency syndrome: clinical, genetic, and therapeutic aspects.
}}