{{Rsnum
|rsid=121908978
|Chromosome=11
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=SLC37A4
|position=119029287
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=SLC37A4
}}{{omim
|id=602671
|rsnum=121908978
|variant=0013
}}{{ClinVar
|rsid=121908978
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=118899997
|CHROM=11
|dbSNPBuildID=133
|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.118899997C>T
|CLNSRC=OMIM Allelic Variant; UniProtKB (variants)
|CLNORIGIN=1
|CLNSRCID=602671.0013; VAR_016840
|CLNSIG=5
|CLNCUI=C0268146
|CLNDBN=Glucose-6-phosphate transport defect; not provided
|Disease=Glucose-6-phosphate transport defect; not provided
|CLNACC=RCV000007345.1; RCV000059144.1
|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=10026167
|Title=Inactivation of the glucose 6-phosphate transporter causes glycogen storage disease type 1b.
}}