| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | KLHL21, LOC126805599 (A462T) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | KLHL21, LOC126805599 (K433R) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126805599, KLHL21 (P411L) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | KLHL21, LOC126805599 (H397R) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | KLHL21, LOC126805599 (S358R) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | KLHL21, LOC126805599 (V352M) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | KLHL21, LOC126805599 (S346T) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
Click to view in NCBI Gene