| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | ATP7B, LOC130009841
+1 more | Single nucleotide variant | not specified +3 more | |
| | | Single nucleotide variant (missense variant) | ALG11-congenital disorder of glycosylation | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
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