| | CLCNKB, LOC106501713 (A77P) | Single nucleotide variant (missense variant) | not provided | |
| | CLCNKB, LOC106501713 (M176V) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CLCNKB, LOC106501713 (R346H +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CLCNKB, LOC106501713 (R365Q +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CLCNKB, LOC106501713 (G246R +1 more) | Single nucleotide variant (missense variant) | not provided | |
| | CLCNKB, LOC106501713 (M243fs +1 more) | Deletion (frameshift variant) | Bartter disease type 3 | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | CLCNKB, LOC106501713 (G301R +1 more) | Single nucleotide variant (missense variant) | Bartter disease type 3 | |
| | CLCNKB, LOC106501713 (F146C +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CLCNKB, LOC106501713 (N313D +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CLCNKB, LOC106501713 (N143K) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CLCNKB, LOC106501713 (R491W +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CLCNKB, LOC106501713 (R365W +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CLCNKB, LOC106501713 (V332M +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CLCNKB, LOC106501713 (T248A +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CLCNKB, LOC106501713 (Q372E +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CLCNKB, LOC106501713 (D363H +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CLCNKB, LOC106501713 (R346C +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CLCNKB, LOC106501713 (E273K +1 more) | Single nucleotide variant (missense variant) | Bartter disease type 3 | |
| | CLCNKB, LOC106501713 (F144S) | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (splice donor variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | CLCNKB, LOC106501713 (R182C) | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | CLCNKB, LOC106501713 (V183fs) | Deletion (frameshift variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Insertion (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | CLCNKB, LOC106501713 (L139R) | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | CLCNKB, LOC106501713 (I113fs +1 more) | Deletion (frameshift variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | CLCNKB, LOC106501713 (H384N +1 more) | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | CLCNKB, LOC106501713 (A254V +1 more) | Single nucleotide variant (missense variant) | not provided | |
| | CLCNKB, LOC106501713 (G219C) | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | CLCNKB, LOC106501713 (T211fs) | Microsatellite (frameshift variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | CLCNKB, LOC106501713 (E199K) | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Deletion (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | CLCNKB, LOC106501713 (L270P +1 more) | Single nucleotide variant (missense variant) | not provided | |
| | | Deletion (inframe_deletion) | not provided | |
| | CLCNKB, LOC106501713 (S60fs +1 more) | Duplication (frameshift variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Indel (splice acceptor variant +1 more) | not provided | |
| | | Duplication (intron variant) | not provided | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | CLCNKB, LOC106501713 (F217L) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CLCNKB, LOC106501713 (A70D) | Single nucleotide variant (missense variant) | Bartter disease type 3 | |
| | CLCNKB, LOC106501713 (S174fs +1 more) | Deletion (frameshift variant) | Bartter disease type 3 | |
| | CLCNKB, LOC106501713 (P124R) | Single nucleotide variant (missense variant) | not specified | |
| | CLCNKB, LOC106501713 (P361S +1 more) | Single nucleotide variant (missense variant) | not provided | |
| | CLCNKB, LOC106501713 (T523I +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CLCNKB, LOC106501713 (M176L) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CLCNKB, LOC106501713 (C157S) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CLCNKB, LOC106501713 (C157S) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CLCNKB, LOC106501713 (T202I +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC106501713, CLCNKB (A204V) | Single nucleotide variant (missense variant) | not provided | |
| | CLCNKB, LOC106501713 (P513L +1 more) | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | CLCNKB, LOC106501713 (G372S +1 more) | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | CLCNKB, LOC106501713 (I326R +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CLCNKB, LOC106501713 (A118T +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CLCNKB, LOC106501713 (P449R +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CLCNKB, LOC106501713 (V567M +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CLCNKB, LOC106501713 (M412V +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CLCNKB, LOC106501713 (S191L +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CLCNKB, LOC106501713 (R103W +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CLCNKB, LOC106501713 (M60T) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CLCNKB, LOC106501713 (A477T +1 more) | Single nucleotide variant (missense variant) | not provided +1 more | |