| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC126863149, TOMM22 (A10V) | Single nucleotide variant (missense variant) | not specified | |
| | LOC126863149, TOMM22 (Q14E) | Single nucleotide variant (missense variant) | not specified | |
| | LOC126863149, TOMM22 (D41G) | Single nucleotide variant (missense variant) | not specified | |
| | LOC126863149, TOMM22 (S61F) | Single nucleotide variant (missense variant) | not specified | |
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