| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | |
| | LOC105371856, TANC2 (S849P +1 more) | Single nucleotide variant (missense variant) | Intellectual developmental disorder with autistic features and language delay, with or without seizures | |
| | | Single nucleotide variant (missense variant) | Intellectual developmental disorder with autistic features and language delay, with or without seizures | |
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