| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | KIF26B, LOC129932922 (G91S) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC129932922, KIF26B (G122R) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | KIF26B, LOC129932922 (L144P) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC129932922, KIF26B (R145S) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
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