{{Rsnum
|rsid=121909135
|Chromosome=1
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=CLCNKB
|position=16051544
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CLCNKA,CLCNKB
}}{{omim
|id=602023
|rsnum=121909135
|variant=0005
}}{{ClinVar
|rsid=121909135
|Reversed=0
|FwdREF=T
|FwdALT=C
|REF=T
|ALT=C
|RSPOS=16051544
|CHROM=1
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000a05000002110100
|GENEINFO=CLCNKB:1188
|GENE_NAME=CLCNKB
|GENE_ID=1188
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.16051544T>C
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_000085.4:c.1294T>C; 602023.0005
|CLNSIG=5
|CLNCUI=C1846343
|CLNDBN=Bartter syndrome type 3
|Disease=Bartter syndrome type 3
|CLNACC=RCV000008033.1
|Tags=PM;NSM;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1846343:607364:ORPHA112
}}