| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | LOC129391025, ZNF554 (G358E) | Single nucleotide variant (missense variant) | not specified | |
| | LOC129391025, ZNF554 (R369C) | Single nucleotide variant (missense variant) | not specified | |
| | LOC129391025, ZNF554 (G386R) | Single nucleotide variant (missense variant) | not specified | |
| | LOC129391025, ZNF554 (S394L) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC129391025, ZNF554 (I401F) | Single nucleotide variant (missense variant) | not specified | |
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