{{Rsnum
|rsid=121909132
|Chromosome=1
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=CLCNKB
|position=16048537
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CLCNKA,CLCNKB
}}{{omim
|id=602023
|rsnum=121909132
|variant=0002
}}{{ClinVar
|rsid=121909132
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=16048537
|CHROM=1
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060020a05000002110100
|GENEINFO=CLCNKB:1188
|GENE_NAME=CLCNKB
|GENE_ID=1188
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.16048537G>A
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_000085.4:c.610G>A; NM_001165945.2:c.-435G>A; 602023.0002
|CLNSIG=5
|CLNCUI=C1846343
|CLNDBN=Bartter syndrome type 3
|Disease=Bartter syndrome type 3
|CLNACC=RCV000008030.1
|Tags=PM;NSM;REF;R5;ASP;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1846343:607364:ORPHA112
}}