{{Rsnum
|rsid=121909136
|Chromosome=1
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=CLCNKB
|position=16055508
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CLCNKA,CLCNKB
}}{{omim
|id=602023
|rsnum=121909136
|variant=0009
}}{{ClinVar
|rsid=121909136
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=16055508
|CHROM=1
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000605000002110100
|GENEINFO=CLCNKB:1188
|GENE_NAME=CLCNKB
|GENE_ID=1188
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.16055508G>A
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_000085.4:c.1830G>A; 602023.0009
|CLNSIG=5
|CLNCUI=C1846344
|CLNDBN=Bartter syndrome, type 3, with hypocalciuria
|Disease=Bartter syndrome
|CLNACC=RCV000008037.1
|Tags=PM;S3D;NSN;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=MedGen
|CLNDSDBID=C1846344
}}