| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | LOC130062906, LOC130062907 +222 more | Copy number loss | See cases | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | APC2, LOC130062956 (A1912V +1 more) | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
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