| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC130064279, SDHAF1 (R16C) | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | |
| | LOC130064279, SDHAF1 (D17H) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC130064279, SDHAF1 (R20C) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (synonymous variant) | Inborn genetic diseases | |
Click to view in NCBI Gene