| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | KANK1, LOC126860554 (R1044H +6 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases +1 more | GConflicting classifications of pathogenicity |
| | KANK1, LOC126860554 (A1141G +6 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | KANK1, LOC126860554 (I1066F +6 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | KANK1, LOC126860554 (D1069G +6 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | KANK1, LOC126860554 (V894F +6 more) | Single nucleotide variant (missense variant +1 more) | not provided +1 more | |
| | KANK1, LOC126860554 (N1076S +6 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases +1 more | |
| | KANK1, LOC126860554 (A1000T +6 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | KANK1, LOC126860554 (A1147T +6 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | KANK1, LOC126860554 (E1158K +6 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases +1 more | |
Click to view in NCBI Gene