{{Rsnum
|rsid=121912668
|Chromosome=22
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=SLC5A1
|position=32043363
|Gene_s=SLC5A1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=182380
|rsnum=121912668
|variant=0001
}}{{ClinVar
|rsid=121912668
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=32439350
|CHROM=22
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=SLC5A1:6523
|GENE_NAME=SLC5A1
|GENE_ID=6523
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000022.10:g.32439350G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=182380.0001
|CLNSIG=5
|CLNCUI=C0268186; C0268151
|CLNDBN=Congenital glucose-galactose malabsorption
|Disease=Congenital glucose-galactose malabsorption
|CLNACC=RCV000013770.23
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0268186:606824:35710:27943000
}}