{{Rsnum
|rsid=80359812
|Chromosome=1
|Orientation=minus
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene=SLC2A1
|position=42943239
|Gene_s=SLC2A1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=80359812
|Reversed=1
|FwdREF=A
|FwdALT=T
|REF=T
|ALT=A
|RSPOS=42943239
|CHROM=1
|dbSNPBuildID=136
|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.42943239T>A
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_006516.2:c.101A>T; 138140.0011
|CLNSIG=5
|CLNCUI=C1847501
|CLNDBN=Dystonia 18
|Disease=Dystonia 18
|CLNACC=RCV000030921.22
|Tags=RV;PM;PMC;SLO;NSM;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1430:C1842534:612126:ORPHA98811
}}{{PMID Auto
|PMID=15622525
|Title=Glut-1 deficiency syndrome: clinical, genetic, and therapeutic aspects.
}}