| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Hemochromatosis type 1 +7 more | |
| | HFE, HFE-AS1 (H63D +1 more) | Single nucleotide variant (non-coding transcript variant +2 more) | not provided +9 more | GPathogenic/Likely pathogenic/Pathogenic, low penetrance; other |
| | | Single nucleotide variant (missense variant +1 more) | Hereditary hemochromatosis +7 more | |
| | | Single nucleotide variant (missense variant +1 more) | Hemochromatosis type 1 +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | HFE-related disorder +19 more | GPathogenic/Pathogenic, low penetrance; other; risk factor |
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