| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC113687175, TFR2 (R541Q +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases +2 more | |
| | | Single nucleotide variant (synonymous variant) | Hereditary hemochromatosis +2 more | GConflicting classifications of pathogenicity |
Click to view in NCBI Gene