| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | BRD7, LOC126862343 (M584K +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | BRD7, LOC126862343 (Q598E +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | BRD7, LOC126862343 (R613* +1 more) | Single nucleotide variant (nonsense) | Granular cell cancer | |
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