| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (synonymous variant) | Mitochondrial complex II deficiency, nuclear type 1 +2 more | |
| | LOC130064281, SDHAF1 (P112S) | Single nucleotide variant (missense variant) | not specified +2 more | GConflicting classifications of pathogenicity |
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