| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | ARMCX5-GPRASP2, LINC00630 | Single nucleotide variant | not specified | |
| | | Copy number loss | Early Onset Neurological Disease Trait | |
| | | Copy number loss | Early Onset Neurological Disease Trait | |
| | | Indel | Heterotaxy, visceral, 1, X-linked | |
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