| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (synonymous variant +1 more) | Citrin deficiency +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | not provided | |
| | | Single nucleotide variant (nonsense +1 more) | not provided +3 more | |
| | | Single nucleotide variant (intron variant) | Citrin deficiency +1 more | GConflicting classifications of pathogenicity |
| | LOC129998833, SLC25A13 (M1T) | Single nucleotide variant (missense variant +2 more) | not provided +6 more | |
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