| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | LOC108281177, SOX2 +1 more | Single nucleotide variant (synonymous variant) | SOX2-related disorder +1 more | |
| | LOC108281177, SOX2 +1 more (N24fs) | Deletion (frameshift variant) | not provided +3 more | |
| | LOC108281177, SOX2 +1 more | Single nucleotide variant (synonymous variant) | SOX2-related disorder | |
| | LOC108281177, SOX2 +1 more | Single nucleotide variant (synonymous variant) | SOX2-related disorder +1 more | |
| | LOC108281177, SOX2 +1 more (L81F) | Single nucleotide variant (missense variant) | SOX2-related disorder | |
| | SOX2-OT, LOC108281177 +1 more | Single nucleotide variant (synonymous variant) | SOX2-related disorder +3 more | |
| | LOC108281177, SOX2 +1 more (A94fs) | Duplication (frameshift variant) | SOX2-related disorder | |
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