{{Rsnum
|rsid = 34188929
|geno1 = (C;C)
|geno2 = (C;T)
|geno3 = (T;T)
|Gene=CLCNKA
|Orientation=plus
|Chromosome=1
|position=16354394
|Assembly=GRCh37
|GenomeBuild=37.1
|dbSNPBuild=131
}}{{Venter SNP
|rsid=34188929
|allele=T
|frequency=
|uid=1103675030580
|type=homozygous_SNP
|hugo=CLCNKB
|ensembl gene=ENSG00000184908
|ensembl transcript=ENST00000375679
|sift=TOLERATED
|disease=Defects in CLCNKB are a cause of Bartter syndrome type 3 (BS type 3) (MIM:607364); also known as classic Bartter syndrome. It is an autosomal recessive form of often severe intravascular volume depletion due to renal salt-wasting associated with low blood pressure, hypokalemic alkalosis, hypercalciuria, and normal serum magnesium levels.
}}