| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (synonymous variant) | not provided +1 more | |
| | ADAM17, IAH1 (S448L +2 more) | Single nucleotide variant (missense variant) | Inflammatory skin and bowel disease, neonatal, 1 +1 more | |
| | | Single nucleotide variant (intron variant) | Inflammatory skin and bowel disease, neonatal, 1 | |
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