{{Rsnum
|rsid=118203980
|Chromosome=1
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=CLDN19
|position=42739895
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CLDN19
}}{{omim
|id=610036
|rsnum=118203980
|variant=0002
}}{{ClinVar
|rsid=118203980
|Reversed=1
|FwdREF=C
|FwdALT=G
|REF=G
|ALT=C
|RSPOS=42739895
|CHROM=1
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000a05000002110100
|GENEINFO=CLDN19:149461
|GENE_NAME=CLDN19
|GENE_ID=149461
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.42739895G>C
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_148960.2:c.169C>G; 610036.0002
|CLNSIG=5
|CLNCUI=C1855466
|CLNDBN=Hypomagnesemia 5, renal, with ocular involvement
|Disease=Hypomagnesemia 5
|CLNACC=RCV000001427.1
|Tags=RV;PM;NSM;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1855466:248190:ORPHA2196
}}