| | LOC126860263, LOC126860264 +4737 more | Copy number loss | See cases | |
| | LOC129999343, LOC129999344 +2213 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number loss | Multiple congenital anomalies/dysmorphic syndrome | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | | Single nucleotide variant (3 prime UTR variant) | Hemochromatosis type 3 | |
| | | Single nucleotide variant (3 prime UTR variant) | Hemochromatosis type 3 | |
| | | Single nucleotide variant (3 prime UTR variant) | Hemochromatosis type 3 | |
| | | Single nucleotide variant (3 prime UTR variant) | Hemochromatosis type 3 | |
| | | Single nucleotide variant (3 prime UTR variant) | Hemochromatosis type 3 | |
| | | Single nucleotide variant (3 prime UTR variant) | Hemochromatosis type 3 | |
| | | Single nucleotide variant (3 prime UTR variant) | Hemochromatosis type 3 | |
| | | Single nucleotide variant (3 prime UTR variant) | Hemochromatosis type 3 | |
| | | Duplication | Hereditary hemochromatosis | |
| | | Single nucleotide variant (3 prime UTR variant) | Hemochromatosis type 3 | |
| | | Single nucleotide variant (synonymous variant) | Hereditary hemochromatosis | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (synonymous variant) | Hereditary hemochromatosis | |
| | | Single nucleotide variant (missense variant) | Hereditary hemochromatosis | |
| | | Single nucleotide variant (synonymous variant) | Hereditary hemochromatosis | |
| | | Single nucleotide variant (synonymous variant) | Hereditary hemochromatosis | |
| | | Single nucleotide variant (synonymous variant) | TFR2-related disorder +1 more | |
| | | Single nucleotide variant (missense variant) | Hemochromatosis type 3 +2 more | |
| | | Single nucleotide variant (synonymous variant) | Hereditary hemochromatosis | |
| | | Single nucleotide variant (synonymous variant) | Hereditary hemochromatosis +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Hereditary hemochromatosis | |
| | | Single nucleotide variant (synonymous variant) | Hereditary hemochromatosis | |
| | | Single nucleotide variant (synonymous variant) | Hereditary hemochromatosis | |
| | | Single nucleotide variant (synonymous variant) | Hereditary hemochromatosis | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (nonsense) | Hemochromatosis type 3 +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (synonymous variant) | Hereditary hemochromatosis | |
| | | Single nucleotide variant (synonymous variant) | Hereditary hemochromatosis | |
| | | Single nucleotide variant (synonymous variant) | Hereditary hemochromatosis | |
| | | Single nucleotide variant (missense variant) | Hemochromatosis type 3 | |
| | | Single nucleotide variant (synonymous variant) | Hereditary hemochromatosis | |
| | | Single nucleotide variant (synonymous variant) | Hereditary hemochromatosis | |
| | | Single nucleotide variant (synonymous variant) | Hereditary hemochromatosis | |
| | | Single nucleotide variant (missense variant) | Hereditary hemochromatosis +1 more | |
| | | Indel (frameshift variant) | Hemochromatosis type 3 | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | |
| | | Single nucleotide variant (missense variant) | Hereditary hemochromatosis | |
| | | Single nucleotide variant (synonymous variant) | Hereditary hemochromatosis | |
| | | Single nucleotide variant (synonymous variant) | Hereditary hemochromatosis | |
| | | Single nucleotide variant (synonymous variant) | Hereditary hemochromatosis | |
| | | Single nucleotide variant (synonymous variant) | Hereditary hemochromatosis | |
| | | Single nucleotide variant (synonymous variant) | Hereditary hemochromatosis | |
| | | Duplication (frameshift variant) | Hereditary hemochromatosis | |
| | | Single nucleotide variant (synonymous variant) | Hereditary hemochromatosis | |
| | | Single nucleotide variant (synonymous variant) | Hereditary hemochromatosis | |
| | | Single nucleotide variant (missense variant) | Hemochromatosis type 3 +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Hereditary hemochromatosis | |
| | | Single nucleotide variant (synonymous variant) | Hereditary hemochromatosis | |
| | | Single nucleotide variant (synonymous variant) | Hereditary hemochromatosis | |
| | | Single nucleotide variant (synonymous variant) | Hereditary hemochromatosis | |
| | | Single nucleotide variant (missense variant) | Hereditary hemochromatosis | |
| | | Single nucleotide variant (synonymous variant) | Hereditary hemochromatosis | |
| | | Single nucleotide variant (synonymous variant) | Hereditary hemochromatosis | |
| | | Single nucleotide variant (synonymous variant) | Hereditary hemochromatosis | |
| | | Single nucleotide variant (synonymous variant) | Hereditary hemochromatosis | |
| | | Single nucleotide variant (missense variant) | Hemochromatosis type 3 +2 more | |
| | | Single nucleotide variant (missense variant) | Hereditary hemochromatosis | |
| | | Single nucleotide variant (synonymous variant) | Hereditary hemochromatosis | |
| | | Single nucleotide variant (synonymous variant) | Hereditary hemochromatosis | |
| | | Single nucleotide variant (missense variant) | Hemochromatosis type 3 | |
| | | Single nucleotide variant (missense variant) | Hereditary hemochromatosis | |
| | | Single nucleotide variant (synonymous variant) | Hereditary hemochromatosis | |
| | | Single nucleotide variant (synonymous variant) | Hereditary hemochromatosis | |
| | | Single nucleotide variant (synonymous variant) | Hereditary hemochromatosis | |
| | | Single nucleotide variant (synonymous variant) | Hereditary hemochromatosis | |
| | | Duplication (frameshift variant) | Hereditary hemochromatosis +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Hereditary hemochromatosis | |
| | | Single nucleotide variant (synonymous variant) | Hereditary hemochromatosis | |
| | | Single nucleotide variant (synonymous variant) | Hereditary hemochromatosis | |
| | | Microsatellite (frameshift variant) | Hereditary hemochromatosis +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Hemochromatosis type 3 | |
| | | Deletion (frameshift variant) | Hemochromatosis type 3 | |
| | | Single nucleotide variant (synonymous variant) | Hereditary hemochromatosis | |
| | | Single nucleotide variant (synonymous variant) | Hereditary hemochromatosis | |
| | | Single nucleotide variant (synonymous variant) | Hereditary hemochromatosis | |
| | | Single nucleotide variant (synonymous variant) | Hereditary hemochromatosis | |
| | | Single nucleotide variant (missense variant) | Hereditary hemochromatosis | |
| | | Single nucleotide variant (synonymous variant) | Hereditary hemochromatosis | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (synonymous variant) | Hereditary hemochromatosis | |
| | | Single nucleotide variant (synonymous variant) | Hereditary hemochromatosis | |
| | | Single nucleotide variant (synonymous variant) | Hereditary hemochromatosis | |
| | | Single nucleotide variant (synonymous variant) | Hereditary hemochromatosis | |
| | | Single nucleotide variant (synonymous variant) | Hereditary hemochromatosis | |
| | | Single nucleotide variant (synonymous variant) | Hereditary hemochromatosis | |
| | | Single nucleotide variant (synonymous variant) | Hereditary hemochromatosis | |
| | | Duplication (frameshift variant) | Hemochromatosis type 3 +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Hemochromatosis type 3 +2 more | |
| | | Single nucleotide variant (synonymous variant) | Hereditary hemochromatosis | |
| | | Single nucleotide variant (synonymous variant) | Hereditary hemochromatosis | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (synonymous variant) | Hereditary hemochromatosis +1 more | GConflicting classifications of pathogenicity |