{{Rsnum
|rsid=386833833
|Chromosome=2
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=LCT
|position=135807214
|Gene_s=LCT
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=2
|CLNACC=RCV000049801.1
|CLNALLE=1
|CLNDBN=Congenital lactase deficiency
|CLNDSDB=MedGen:OMIM:SNOMED_CT
|CLNDSDBID=C0268179:223000:5388008
|CLNHGVS=NC_000002.11:g.136564784C>T
|CLNSIG=4
|Disease=Congenital lactase deficiency
|FwdALT=A
|FwdREF=G
|REF=C
|RSPOS=136564784
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;PMC;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050068000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=386833833
|GENEINFO=LCT:3938
|GENE_ID=3938
|GENE_NAME=LCT
}}{{PMID Auto
|PMID=16400612
|Title=Mutations in the translated region of the lactase gene (LCT) underlie congenital lactase deficiency.
|OA=1
}}