| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | BAZ1B, LOC129998587 (P17A) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | BAZ1B, LOC129998587 (P26A) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | BAZ1B, LOC129998587 (L16F) | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
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