| | | Duplication (frameshift variant) | Marfan syndrome | |
| | | Single nucleotide variant (nonsense) | Marfan syndrome | |
| | | Deletion (frameshift variant) | Marfan Syndrome/Loeys-Dietz Syndrome/Familial Thoracic Aortic Aneurysms and Dissections +3 more | GPathogenic/Likely pathogenic |
| | | Duplication (frameshift variant) | Marfan syndrome +1 more | |
| | | Single nucleotide variant (nonsense) | Cardiovascular phenotype +2 more | |
| | | Deletion (frameshift variant) | Marfan syndrome | |
| | | Single nucleotide variant (missense variant) | Marfan syndrome | |
| | | Single nucleotide variant (missense variant) | Marfan syndrome +1 more | |
| | | Deletion (frameshift variant) | Marfan syndrome | |
| | | Duplication (frameshift variant) | Marfan syndrome | |
| | | Deletion (frameshift variant) | Marfan syndrome | |
| | | Single nucleotide variant (missense variant) | Marfan syndrome +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Marfan syndrome | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Marfan syndrome | |
| | | Single nucleotide variant (missense variant) | Marfan syndrome | |
| | | Single nucleotide variant (nonsense) | Isolated thoracic aortic aneurysm +3 more | GPathogenic/Likely pathogenic |
| | | Duplication (frameshift variant) | Marfan syndrome | |
| | | Single nucleotide variant (missense variant) | not provided +9 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (splice donor variant) | not provided +3 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Familial thoracic aortic aneurysm and aortic dissection +1 more | |
| | | Single nucleotide variant (missense variant) | not specified +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Geleophysic dysplasia +8 more | GConflicting classifications of pathogenicity |
| | | Duplication (nonsense) | not provided | |
| | | Insertion (frameshift variant) | Marfan syndrome | |
| | | Single nucleotide variant (nonsense) | Cardiovascular phenotype | |
| | | Single nucleotide variant (missense variant) | not specified +8 more | GConflicting classifications of pathogenicity |
| | | Duplication (nonsense) | Marfan syndrome +1 more | |
| | | Single nucleotide variant (nonsense) | Marfan syndrome | |
| | | Single nucleotide variant (missense variant) | Marfan syndrome | |
| | | Single nucleotide variant (missense variant) | Marfan syndrome +3 more | |
| | | Indel | Marfan syndrome | |
| | | Single nucleotide variant (missense variant) | Marfan syndrome +3 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Marfan syndrome | |
| | | Single nucleotide variant (missense variant) | Marfan syndrome +1 more | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Familial thoracic aortic aneurysm and aortic dissection +2 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | not provided +2 more | |
| | | Single nucleotide variant (missense variant) | Marfan syndrome +1 more | |
| | | Duplication (frameshift variant) | Marfan syndrome +1 more | |
| | | Single nucleotide variant (missense variant) | Marfan syndrome | |
| | | Deletion (frameshift variant) | Marfan syndrome | |
| | | Single nucleotide variant (missense variant) | Marfan syndrome | |
| | | Indel | Marfan syndrome | |
| | | Single nucleotide variant (nonsense) | Marfan syndrome +1 more | |
| | | Single nucleotide variant (missense variant) | not provided +3 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Marfan syndrome +1 more | |
| | | Single nucleotide variant (missense variant) | Marfan syndrome +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Marfan syndrome +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Marfan syndrome | |
| | | Single nucleotide variant (missense variant) | Marfan Syndrome/Loeys-Dietz Syndrome/Familial Thoracic Aortic Aneurysms and Dissections +3 more | |
| | | Single nucleotide variant (missense variant) | Marfan syndrome +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Marfan syndrome +1 more | |
| | | Single nucleotide variant (missense variant) | Marfan syndrome | |
| | | Single nucleotide variant (missense variant) | Familial thoracic aortic aneurysm and aortic dissection +9 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Marfan syndrome | |
| | | Single nucleotide variant (missense variant) | Familial thoracic aortic aneurysm and aortic dissection +8 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Marfan syndrome | |
| | | Single nucleotide variant (missense variant) | Isolated thoracic aortic aneurysm +10 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Marfan syndrome +2 more | |
| | | Single nucleotide variant (intron variant) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (splice donor variant) | Marfan syndrome +2 more | |
| | | Deletion (inframe_deletion) | Marfan syndrome +1 more | |
| | | Duplication (frameshift variant) | Marfan syndrome | |
| | | Deletion (frameshift variant) | Marfan syndrome | |
| | | Single nucleotide variant (nonsense) | Marfan syndrome | |
| | | Single nucleotide variant (missense variant) | Connective tissue dysplasia +11 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (synonymous variant) | Marfan syndrome | |
| | | Single nucleotide variant (missense variant) | Familial thoracic aortic aneurysm and aortic dissection | |
| | | Single nucleotide variant (missense variant) | Isolated thoracic aortic aneurysm +5 more | GConflicting classifications of pathogenicity |
| | | Deletion (frameshift variant) | Marfan syndrome | |
| | | Single nucleotide variant (missense variant) | Marfan syndrome | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (intron variant) | not provided +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (splice donor variant) | Marfan syndrome +1 more | GPathogenic/Likely pathogenic |
| | | Deletion (frameshift variant) | Marfan syndrome | |
| | | Duplication (frameshift variant) | Marfan syndrome | |
| | | Single nucleotide variant (missense variant) | Marfan syndrome +3 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Marfan syndrome | |
| | | Deletion (frameshift variant) | Marfan syndrome | |
| | | Deletion (frameshift variant) | Marfan syndrome | |
| | | Single nucleotide variant (nonsense) | Marfan syndrome | |
| | | Single nucleotide variant (missense variant) | Marfan syndrome | |
| | | Single nucleotide variant (missense variant) | Marfan syndrome +2 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Marfan syndrome +3 more | |
| | | Single nucleotide variant (missense variant) | Marfan syndrome +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Marfan syndrome +1 more | |
| | | Single nucleotide variant (missense variant) | Marfan syndrome | |
| | | Single nucleotide variant (missense variant) | Marfan syndrome | |
| | | Single nucleotide variant (missense variant) | Marfan syndrome | |
| | | Single nucleotide variant (missense variant) | Marfan syndrome +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (nonsense) | Marfan syndrome | |
| | | Single nucleotide variant (missense variant) | not specified +10 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Familial thoracic aortic aneurysm and aortic dissection +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Marfan syndrome +1 more | |
| | | Single nucleotide variant (missense variant) | Familial thoracic aortic aneurysm and aortic dissection | |
| | | Single nucleotide variant (nonsense) | Marfan syndrome +1 more | |
| | | Single nucleotide variant (missense variant) | not specified +4 more | |
| | | Duplication (frameshift variant) | Marfan syndrome +1 more | |
| | | Single nucleotide variant (splice acceptor variant) | Marfan syndrome | |
| | | Single nucleotide variant (missense variant) | Marfan syndrome +1 more | |