| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC126861888, CHD8 (E2067K +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases +2 more | |
| | CHD8, LOC126861888 (T2034A +1 more) | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided +1 more | |
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