| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | ALDH5A1, GPLD1
+1 more (G11E) | Single nucleotide variant (missense variant) | Inborn genetic diseases +2 more | GConflicting classifications of pathogenicity |
| | ALDH5A1, GPLD1
+1 more (S17L) | Single nucleotide variant (missense variant) | Inborn genetic diseases +2 more | |
| | ALDH5A1, GPLD1
+1 more (C93F) | Single nucleotide variant (missense variant) | Succinate-semialdehyde dehydrogenase deficiency +1 more | |
Click to view in NCBI Gene