| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | AUTS2, LOC129998550 (L30R) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | AUTS2, LOC129998550 (A34T) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | AUTS2, LOC129998550 (G36R) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
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