| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC129390190, LOC129390191
+610 more | Copy number loss | See cases | |
| | DNA2, LOC132089842 (D1041G) | Single nucleotide variant (missense variant +1 more) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Deletion (intron variant) | not provided | |
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