| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC130064281, SDHAF1 (P85S) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC130064281, SDHAF1 (D94del) | Microsatellite (inframe_deletion) | Inborn genetic diseases | |
| | LOC130064281, SDHAF1 (R99S) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (synonymous variant) | not provided +1 more | |
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