| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC130064656, TOMM40 (P58S) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130064656, TOMM40 (G24E) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130064656, TOMM40 (S43T) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130064656, TOMM40 (S49R) | Single nucleotide variant (missense variant) | not provided | |
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