| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | FOXRED1, LOC130007026 (G9D) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | FOXRED1, LOC130007026 (R17Q) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases +2 more | |
Click to view in NCBI Gene