| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | LOC130062841, RNF126 (P8A) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130062841, RNF126 (H7R) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130062841, RNF126 (S17Y) | Single nucleotide variant (missense variant) | not specified | |
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