| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | GTF2IRD2B, LOC106029313 (S7P +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | GTF2IRD2B, LOC106029313 (V56A +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | GTF2IRD2B, LOC106029313 (S178P +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | GTF2IRD2B, LOC106029313 (T232M +1 more) | Single nucleotide variant (missense variant) | not specified | |
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