{{Rsnum
|rsid=121908543
|Chromosome=3
|Orientation=plus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=CLDN16
|position=190409949
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CLDN16
}}{{omim
|id=603959
|rsnum=121908543
|variant=0016
}}{{ClinVar
|rsid=121908543
|Reversed=0
|FwdREF=T
|FwdALT=G
|REF=T
|ALT=G
|RSPOS=190127738
|CHROM=3
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=CLDN16:10686
|GENE_NAME=CLDN16
|GENE_ID=10686
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000003.11:g.190127738T>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=603959.0016
|CLNSIG=5
|CLNCUI=C0268448
|CLNDBN=Primary hypomagnesemia
|Disease=Primary hypomagnesemia
|CLNACC=RCV000006303.1
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0268448:248250:31043:80710001
}}