| | LOC126860768, LOC126860769 +3785 more | Copy number gain | See cases | |
| | LOC124310660, LOC124310661 +3784 more | Copy number gain | See cases | |
| | LOC111413024, LOC111413033 +3785 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | LOC116216098, LOC116216099 +3785 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | LOC126860765, LOC126860766 +3785 more | Copy number gain | See cases | |
| | LOC130002043, LOC130002044 +1072 more | Copy number gain | See cases | |
| | LOC126860637, LOC126860638 +1188 more | Copy number gain | See cases | |
| | LOC130002218, LOC130002219 +994 more | Copy number gain | See cases | |
| | LOC130002205, LOC130002206 +417 more | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | Weiss-kruszka syndrome | |
| | | Copy number loss | See cases | |
| | LOC132089619, LOC132089620 +310 more | Copy number loss | See cases | |
| | | Copy number gain | See cases | |
| | | Single nucleotide variant | Familial High Density Lipoprotein Deficiency +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Tangier disease +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Tangier disease +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Hypoalphalipoproteinemia, primary, 1 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Tangier disease +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Hypoalphalipoproteinemia, primary, 1 +1 more | |
| | | Deletion (3 prime UTR variant) | Familial High Density Lipoprotein Deficiency +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Tangier disease +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Tangier disease +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | Tangier disease +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Tangier disease +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Hypoalphalipoproteinemia, primary, 1 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Hypoalphalipoproteinemia, primary, 1 +1 more | GConflicting classifications of pathogenicity |
| | | Deletion (3 prime UTR variant) | not provided | |
| | | Single nucleotide variant (3 prime UTR variant) | Hypoalphalipoproteinemia, primary, 1 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Tangier disease +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Hypoalphalipoproteinemia, primary, 1 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Tangier disease +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Hypoalphalipoproteinemia, primary, 1 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Hypoalphalipoproteinemia, primary, 1 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Tangier disease +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | Hypoalphalipoproteinemia, primary, 1 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Hypoalphalipoproteinemia, primary, 1 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Tangier disease +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Tangier disease +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | Hypoalphalipoproteinemia, primary, 1 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Tangier disease +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | Hypoalphalipoproteinemia, primary, 1 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Hypoalphalipoproteinemia, primary, 1 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Tangier disease +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Hypoalphalipoproteinemia, primary, 1 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Hypoalphalipoproteinemia, primary, 1 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Tangier disease +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | Hypoalphalipoproteinemia, primary, 1 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Hypoalphalipoproteinemia, primary, 1 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Hypoalphalipoproteinemia, primary, 1 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | not provided +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Hypoalphalipoproteinemia, primary, 1 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | not provided +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Tangier disease +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Tangier disease +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Hypoalphalipoproteinemia, primary, 1 +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | Hypoalphalipoproteinemia, primary, 1 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Hypoalphalipoproteinemia, primary, 1 +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | Hypoalphalipoproteinemia, primary, 1 +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | Hypoalphalipoproteinemia, primary, 1 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | not provided +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Hypoalphalipoproteinemia, primary, 1 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Hypoalphalipoproteinemia, primary, 1 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Hypoalphalipoproteinemia, primary, 1 +1 more | GConflicting classifications of pathogenicity |
| | | Duplication (3 prime UTR variant) | not provided | |
| | | Single nucleotide variant (3 prime UTR variant) | Hypoalphalipoproteinemia, primary, 1 +1 more | |
| | | Deletion (3 prime UTR variant) | Familial High Density Lipoprotein Deficiency +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | not provided +2 more | |
| | | Duplication (3 prime UTR variant) | Familial High Density Lipoprotein Deficiency +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Familial High Density Lipoprotein Deficiency +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Tangier disease +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Hypoalphalipoproteinemia, primary, 1 +1 more | |
| | | Deletion (3 prime UTR variant) | Familial High Density Lipoprotein Deficiency +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Tangier disease +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | Tangier disease +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Hypoalphalipoproteinemia, primary, 1 +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | Hypoalphalipoproteinemia, primary, 1 +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | Hypoalphalipoproteinemia, primary, 1 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Hypoalphalipoproteinemia, primary, 1 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Tangier disease +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | Hypoalphalipoproteinemia, primary, 1 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Hypoalphalipoproteinemia, primary, 1 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Hypoalphalipoproteinemia, primary, 1 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Hypoalphalipoproteinemia, primary, 1 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Hypoalphalipoproteinemia, primary, 1 +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | Tangier disease +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | not provided +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Familial High Density Lipoprotein Deficiency +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Tangier disease +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Hypoalphalipoproteinemia, primary, 1 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Hypoalphalipoproteinemia, primary, 1 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Tangier disease +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Hypoalphalipoproteinemia, primary, 1 +1 more | GConflicting classifications of pathogenicity |