| | | Single nucleotide variant (intron variant) | Familial amyloid neuropathy +3 more | |
| | | Single nucleotide variant (missense variant) | Hyperthyroxinemia, dystransthyretinemic +2 more | |
| | | Single nucleotide variant (missense variant) | Familial amyloid neuropathy +2 more | |
| | | Single nucleotide variant (missense variant) | Familial amyloid neuropathy +3 more | |
| | | Single nucleotide variant (5 prime UTR variant) | not provided +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Hyperthyroxinemia, dystransthyretinemic +3 more | |
| | | Single nucleotide variant (missense variant) | Familial amyloid neuropathy +3 more | |
| | | | Familial amyloid neuropathy | |
| | | Single nucleotide variant (missense variant) | Familial amyloid neuropathy +3 more | |
| | | Single nucleotide variant (missense variant) | Tip-toe gait +5 more | |
| | | Single nucleotide variant | Familial amyloid neuropathy +2 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +4 more | |
| | | Deletion (inframe_deletion) | Familial amyloid neuropathy +2 more | |
| | | Single nucleotide variant (missense variant) | Hyperthyroxinemia, dystransthyretinemic +2 more | |
| | | Single nucleotide variant (missense variant) | Familial amyloid neuropathy +3 more | |
| | | Single nucleotide variant (missense variant) | Familial amyloid neuropathy +3 more | |
| | | Single nucleotide variant (synonymous variant) | Carpal tunnel syndrome 1 +3 more | |
| | | Single nucleotide variant (synonymous variant) | Familial amyloid neuropathy +4 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +9 more | |
| | | Single nucleotide variant (intron variant) | not specified +3 more | |
| | | Single nucleotide variant (intron variant) | not specified +4 more | |
| | | Single nucleotide variant (synonymous variant) | Carpal tunnel syndrome 1 +4 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Hyperthyroxinemia, dystransthyretinemic +2 more | |
| | | Duplication (inframe_insertion) | Hyperthyroxinemia, dystransthyretinemic +4 more | |
| | | Single nucleotide variant | Hyperthyroxinemia, dystransthyretinemic +2 more | |
| | | Single nucleotide variant (missense variant) | Familial amyloid neuropathy +3 more | |
| | | Single nucleotide variant (missense variant) | Familial amyloid neuropathy +8 more | |
| | | Single nucleotide variant (missense variant) | not specified +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Familial amyloid neuropathy +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not specified +5 more | |
| | | Single nucleotide variant (intron variant) | not specified +5 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +5 more | |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy +6 more | |
| | | Single nucleotide variant (missense variant) | Familial amyloid neuropathy +4 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Familial amyloid neuropathy +6 more | |
| | | Single nucleotide variant (missense variant) | Familial amyloid neuropathy +6 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Carpal tunnel syndrome 1 | |
| | | Single nucleotide variant (missense variant) | Familial amyloid neuropathy +4 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Familial amyloid neuropathy +12 more | |
| | | Single nucleotide variant (missense variant) | Familial amyloid neuropathy +6 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy +7 more | |