| | | Single nucleotide variant (missense variant) | not provided +1 more | GConflicting classifications of pathogenicity |
| | CLCNKB, LOC106501713 (V58L) | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | GConflicting classifications of pathogenicity |
| | CLCNKB, LOC106501713 (M60T) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CLCNKB, LOC106501713 (S113T) | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | |
| | CLCNKB, LOC106501713 (M129V) | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | |
| | CLCNKB, LOC106501713 (C157S) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CLCNKB, LOC106501713 (C157S) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CLCNKB, LOC106501713 (M176L) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CLCNKB, LOC106501713 (A178V) | Single nucleotide variant (missense variant) | not provided +1 more | |
| | CLCNKB, LOC106501713 (F217L) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CLCNKB, LOC106501713 (R103W +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CLCNKB, LOC106501713 (A118T +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC106501713, CLCNKB (S191L +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CLCNKB, LOC106501713 (T202I +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CLCNKB, LOC106501713 (I229V +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | GConflicting classifications of pathogenicity |
| | CLCNKB, LOC106501713 (M412V +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC106501713, CLCNKB (P449R +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CLCNKB, LOC106501713 (V284M +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | |
| | CLCNKB, LOC106501713 (N459H +1 more) | Single nucleotide variant (missense variant) | Bartter disease type 3 +3 more | |
| | CLCNKB, LOC106501713 (A300T +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | GConflicting classifications of pathogenicity |
| | CLCNKB, LOC106501713 (A477T +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CLCNKB, LOC106501713 (A319D +1 more) | Single nucleotide variant (missense variant) | Bartter disease type 3 +3 more | |
| | CLCNKB, LOC106501713 (I326R +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CLCNKB, LOC106501713 (T523I +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CLCNKB, LOC106501713 (I525T +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases +3 more | |
| | CLCNKB, LOC106501713 (V567M +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC106501713, CLCNKB (S404P +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | GConflicting classifications of pathogenicity |