| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | COMMD1, LOC129933847 (H25R) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | COMMD1, LOC129933847 (P28L) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | COMMD1, LOC129933847 (L39P) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Copy number loss | not provided | |
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