| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | ABCB10, LOC129932735 (W68C) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ABCB10, LOC129932735 (L51R) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ABCB10, LOC129932735 (P37R) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ABCB10, LOC129932735 (P14R) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
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