| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | ANKRD34A, ANKRD35 +42 more | Copy number loss | See cases | |
| | LIX1L-AS1, LOC126805851 +1 more | Single nucleotide variant (non-coding transcript variant +1 more) | not provided +2 more | GConflicting classifications of pathogenicity; other |
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