| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | ARHGEF35-AS1, OR2A42 (V68I) | Single nucleotide variant (missense variant) | not provided | |
| | ARHGEF35-AS1, OR2A42 (T56P) | Single nucleotide variant (missense variant) | not specified | |
| | ARHGEF35-AS1, OR2A42 (H55P) | Single nucleotide variant (missense variant) | not specified | |
| | ARHGEF35-AS1, OR2A42 (T37I) | Single nucleotide variant (missense variant) | not specified | |
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