| | | Single nucleotide variant (nonsense) | Familial visceral amyloidosis, Ostertag type | |
| | | Deletion (frameshift variant) | Familial visceral amyloidosis, Ostertag type | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Familial visceral amyloidosis, Ostertag type | |
| | | Single nucleotide variant (intron variant) | not specified +4 more | |
| | | Single nucleotide variant (intron variant) | Hypoproteinemia, hypercatabolic +1 more | |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype +4 more | |
| | | Single nucleotide variant (synonymous variant) | Familial visceral amyloidosis, Ostertag type +4 more | |
| | | Single nucleotide variant (intron variant) | Familial visceral amyloidosis, Ostertag type +1 more | |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype +4 more | |
| | | Single nucleotide variant (intron variant) | Familial visceral amyloidosis, Ostertag type +1 more | |
| | | Single nucleotide variant (synonymous variant) | Familial visceral amyloidosis, Ostertag type +3 more | |
| | | Single nucleotide variant (missense variant) | Familial visceral amyloidosis, Ostertag type +3 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +4 more | |
| | APOA1, APOA1-AS (D18N +1 more) | Single nucleotide variant (non-coding transcript variant +1 more) | not provided +4 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Hypoproteinemia, hypercatabolic +1 more | |
| | | Single nucleotide variant (missense variant +2 more) | not provided +5 more | |
| | | Single nucleotide variant (nonsense) | not specified +2 more | |
| | | Single nucleotide variant (missense variant) | not specified +2 more | |
| | | Duplication (frameshift variant) | Familial visceral amyloidosis, Ostertag type | |
| | | Single nucleotide variant (splice donor variant) | Congenital afibrinogenemia +2 more | |
| | | Single nucleotide variant (nonsense) | Familial visceral amyloidosis, Ostertag type +2 more | |
| | | Single nucleotide variant (intron variant) | not provided +3 more | |
| | | Single nucleotide variant (intron variant) | not provided +3 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +5 more | |
| | | Indel (missense variant) | Hypoproteinemia, hypercatabolic | |
| | | Single nucleotide variant (missense variant) | not provided +3 more | |
| | | Single nucleotide variant (missense variant) | Familial visceral amyloidosis, Ostertag type | |
| | | Single nucleotide variant (missense variant) | Familial visceral amyloidosis, Ostertag type | |
| | | Single nucleotide variant (missense variant +1 more) | Familial visceral amyloidosis, Ostertag type +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Familial visceral amyloidosis, Ostertag type +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Familial visceral amyloidosis, Ostertag type +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Familial visceral amyloidosis, Ostertag type +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | not specified +3 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Familial visceral amyloidosis, Ostertag type +1 more | |
| | | Single nucleotide variant (missense variant) | Familial visceral amyloidosis, Ostertag type +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | Familial visceral amyloidosis, Ostertag type | |
| | | Single nucleotide variant (3 prime UTR variant) | Familial visceral amyloidosis, Ostertag type | |
| | | Single nucleotide variant (3 prime UTR variant) | Familial visceral amyloidosis, Ostertag type | |
| | | Single nucleotide variant (3 prime UTR variant) | Familial visceral amyloidosis, Ostertag type | |
| | | Single nucleotide variant (missense variant) | Familial visceral amyloidosis, Ostertag type | |
| | | Single nucleotide variant (3 prime UTR variant) | Familial visceral amyloidosis, Ostertag type | |
| | | Single nucleotide variant (3 prime UTR variant) | Familial visceral amyloidosis, Ostertag type | |
| | | Single nucleotide variant (3 prime UTR variant) | Familial visceral amyloidosis, Ostertag type | |
| | | Single nucleotide variant (nonsense) | Familial visceral amyloidosis, Ostertag type | |
| | | Single nucleotide variant (missense variant) | Familial visceral amyloidosis, Ostertag type +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Familial visceral amyloidosis, Ostertag type | |
| | | Single nucleotide variant (3 prime UTR variant) | Familial visceral amyloidosis, Ostertag type | |
| | | Single nucleotide variant (3 prime UTR variant) | Familial visceral amyloidosis, Ostertag type | |
| | | Single nucleotide variant (3 prime UTR variant) | Familial visceral amyloidosis, Ostertag type | |
| | | Single nucleotide variant (3 prime UTR variant) | Familial visceral amyloidosis, Ostertag type | |
| | | Single nucleotide variant (3 prime UTR variant) | Familial visceral amyloidosis, Ostertag type | |
| | | Single nucleotide variant (3 prime UTR variant) | Familial visceral amyloidosis, Ostertag type | |
| | | Single nucleotide variant (missense variant) | Hypoalphalipoproteinemia, primary, 1 +1 more | |
| | | Single nucleotide variant (missense variant) | not specified +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Hypoalphalipoproteinemia, primary, 1 +1 more | |
| | | Single nucleotide variant (missense variant) | Hypoalphalipoproteinemia, primary, 1 +1 more | |
| | | Single nucleotide variant (5 prime UTR variant) | Hypoalphalipoproteinemia, primary, 1 +1 more | |
| | | Single nucleotide variant (synonymous variant) | Hypoalphalipoproteinemia, primary, 1 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Hypoalphalipoproteinemia, primary, 1 +1 more | |
| | | Single nucleotide variant (missense variant) | Familial visceral amyloidosis, Ostertag type | |
| | | Deletion (frameshift variant) | Familial visceral amyloidosis, Ostertag type | |
| | | Single nucleotide variant (synonymous variant) | not provided +5 more | |
| | | Single nucleotide variant (missense variant) | not provided +4 more | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Familial visceral amyloidosis, Ostertag type +4 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +3 more | |
| | | Single nucleotide variant (missense variant) | not provided +2 more | |
| | | Single nucleotide variant (synonymous variant) | Familial visceral amyloidosis, Ostertag type +4 more | |
| | | Single nucleotide variant (missense variant) | Familial visceral amyloidosis, Ostertag type | |
| | APOA1-AS, APOA1 (K131del +1 more) | Microsatellite (inframe_deletion +2 more) | Chronic kidney disease +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not specified +4 more | |
| | | Single nucleotide variant (nonsense) | Familial visceral amyloidosis, Ostertag type +3 more | GPathogenic/Likely pathogenic |
| | | Deletion (frameshift variant) | Familial visceral amyloidosis, Ostertag type | |
| | | Single nucleotide variant (nonsense) | not provided +4 more | GPathogenic/Likely pathogenic |
| | | Microsatellite (frameshift variant) | Hypoalphalipoproteinemia, primary, 2, intermediate +3 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (nonsense) | Familial visceral amyloidosis, Ostertag type +3 more | |
| | | Single nucleotide variant | not provided +2 more | |
| | | Single nucleotide variant (missense variant) | Familial visceral amyloidosis, Ostertag type +2 more | |
| | | Single nucleotide variant (missense variant) | Familial visceral amyloidosis, Ostertag type +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Congenital afibrinogenemia +3 more | |
| | | Single nucleotide variant (synonymous variant) | not specified +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Familial visceral amyloidosis, Ostertag type +1 more | |
| | | Single nucleotide variant (missense variant) | Familial visceral amyloidosis, Ostertag type +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Familial visceral amyloidosis, Ostertag type +1 more | |
| | | Single nucleotide variant (synonymous variant) | Familial visceral amyloidosis, Ostertag type +1 more | |
| | | Single nucleotide variant (synonymous variant) | Familial visceral amyloidosis, Ostertag type +1 more | |
| | | Single nucleotide variant (missense variant) | Familial visceral amyloidosis, Ostertag type +3 more | |
| | | Single nucleotide variant (missense variant) | Familial visceral amyloidosis, Ostertag type +2 more | |
| | | Single nucleotide variant (missense variant) | Familial visceral amyloidosis, Ostertag type +2 more | |
| | | Single nucleotide variant (missense variant) | Familial visceral amyloidosis, Ostertag type +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Familial visceral amyloidosis, Ostertag type +2 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +2 more | |
| | | Single nucleotide variant (missense variant) | Familial visceral amyloidosis, Ostertag type +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Familial visceral amyloidosis, Ostertag type +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Familial visceral amyloidosis, Ostertag type +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | Familial visceral amyloidosis, Ostertag type +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | not provided +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Familial visceral amyloidosis, Ostertag type | |
| | | Deletion (3 prime UTR variant) | Familial visceral amyloidosis, Ostertag type | |