{{Rsnum
|rsid=80359814
|Chromosome=1
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=SLC2A1
|position=42931049
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=SLC2A1
}}{{omim
|id=138140
|rsnum=80359814
|variant=0006
}}{{ClinVar
|rsid=80359814
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=42931049
|CHROM=1
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050168000a05000002110100
|GENEINFO=SLC2A1:6513
|GENE_NAME=SLC2A1
|GENE_ID=6513
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.42931049C>T
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_006516.2:c.272G>A; 138140.0006
|CLNSIG=5
|CLNCUI=C1847501
|CLNDBN=Glucose transporter type 1 deficiency syndrome
|Disease=Glucose transporter type 1 deficiency syndrome
|CLNACC=RCV000017490.27
|Tags=RV;PM;PMC;SLO;NSM;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1430:C1847501:606777:ORPHA71277
}}{{PMID Auto
|PMID=11136715
|Title=Autosomal dominant transmission of GLUT1 deficiency.
}}