| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | H2BC17, LOC129996150 (G27S) | Single nucleotide variant (missense variant) | not specified | |
| | H2BC17, LOC129996150 (G27R) | Single nucleotide variant (missense variant) | not specified | |
| | H2BC17, LOC129996150 (P11L) | Single nucleotide variant (missense variant) | not specified | |
| | H2BC17, LOC129996150 (K13R) | Single nucleotide variant (missense variant) | not specified | |
| | H2BC17, LOC129996150 (D3E) | Single nucleotide variant (missense variant) | not specified | |
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