| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | CHCHD6, LOC123038169 (R162H +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | CHCHD6, LOC123038169 (R150C +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | CHCHD6, LOC123038169 (R152C +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | CHCHD6, LOC123038169 (K165Q +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | | Copy number loss | not provided | |
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