{{Rsnum
|rsid=121912669
|Chromosome=22
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=SLC5A1
|position=32043364
|Gene_s=SLC5A1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=182380
|rsnum=121912669
|variant=0002
}}{{ClinVar
|rsid=121912669
|Reversed=0
|FwdREF=A
|FwdALT=G
|REF=A
|ALT=G
|RSPOS=32439351
|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.32439351A>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=182380.0002
|CLNSIG=5
|CLNCUI=C0268186
|CLNDBN=Congenital glucose-galactose malabsorption
|Disease=Congenital glucose-galactose malabsorption
|CLNACC=RCV000013771.22
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0268186:606824:35710:27943000
}}