| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | KDM5B, LOC129932250 (P20L) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | KDM5B, LOC129932250 (P20A) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | KDM5B, LOC129932250 (P11Q) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
Click to view in NCBI Gene