| | | Single nucleotide variant (missense variant) | Ehlers-Danlos syndrome, type 4 +2 more | |
| | | Single nucleotide variant (genic upstream transcript variant +1 more) | Marfan syndrome +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (genic upstream transcript variant +1 more) | Loeys-Dietz syndrome 2 +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (5 prime UTR variant) | Malignant tumor of esophagus +5 more | GUncertain significance/Uncertain risk allele |
| | | Single nucleotide variant (missense variant) | Familial thoracic aortic aneurysm and aortic dissection +6 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Familial thoracic aortic aneurysm and aortic dissection +5 more | |
| | | Single nucleotide variant (missense variant) | not provided +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Marfan syndrome +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | Ectopia lentis 1, isolated, autosomal dominant +10 more | |
| | | Single nucleotide variant (missense variant) | not provided +9 more | |
| | | Single nucleotide variant (missense variant) | Stiff skin syndrome +9 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Familial thoracic aortic aneurysm and aortic dissection +9 more | |
| | | Single nucleotide variant (missense variant) | Marfan syndrome +8 more | |
| | | Single nucleotide variant (missense variant) | Marfan syndrome +10 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Marfan syndrome +9 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Marfan syndrome +10 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | not specified +9 more | |
| | | Single nucleotide variant (missense variant) | Marfan syndrome +9 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not specified +10 more | |
| | | Single nucleotide variant (missense variant) | Marfan syndrome +8 more | |
| | | Single nucleotide variant (missense variant) | Familial thoracic aortic aneurysm and aortic dissection +9 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Familial thoracic aortic aneurysm and aortic dissection +10 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Familial thoracic aortic aneurysm and aortic dissection +8 more | |
| | | 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 +8 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not specified +9 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Marfan syndrome +9 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Connective tissue dysplasia +12 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Geleophysic dysplasia 2 +8 more | |
| | | Single nucleotide variant (missense variant) | Marfan syndrome +8 more | |
| | | Single nucleotide variant (missense variant) | Acromicric dysplasia +9 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Ectopia lentis 1, isolated, autosomal dominant +8 more | |
| | | Single nucleotide variant (synonymous variant) | not specified +9 more | |
| | | Single nucleotide variant (missense variant) | not provided +9 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Stiff skin syndrome +7 more | |
| | | Single nucleotide variant (missense variant) | not specified +10 more | |
| | | Single nucleotide variant (missense variant) | Marfan syndrome +9 more | |
| | | Single nucleotide variant (missense variant) | Ectopia lentis 1, isolated, autosomal dominant +10 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Marfan syndrome +9 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Familial thoracic aortic aneurysm and aortic dissection +8 more | |
| | | Single nucleotide variant (missense variant) | Acromicric dysplasia +10 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Familial thoracic aortic aneurysm and aortic dissection +9 more | |
| | | Single nucleotide variant (missense variant) | Marfan syndrome +9 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | FBN1-related disorder +9 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +10 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Familial thoracic aortic aneurysm and aortic dissection +10 more | |
| | | Single nucleotide variant (missense variant) | Marfan syndrome +10 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +10 more | |
| | | Single nucleotide variant (missense variant) | not provided +12 more | |
| | | Single nucleotide variant (missense variant) | Geleophysic dysplasia 2 +8 more | |
| | | Single nucleotide variant (missense variant) | Marfan syndrome +11 more | GConflicting classifications of pathogenicity |
| | | 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 +9 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Marfan syndrome +8 more | |
| | | Single nucleotide variant (missense variant) | not provided +10 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Ectopia lentis 1, isolated, autosomal dominant +8 more | |
| | | Single nucleotide variant (missense variant) | Marfan syndrome +9 more | |
| | | Single nucleotide variant (missense variant) | not specified +9 more | |
| | | Single nucleotide variant (missense variant) | MASS syndrome +8 more | |
| | | Single nucleotide variant (missense variant) | Familial thoracic aortic aneurysm and aortic dissection +10 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Familial thoracic aortic aneurysm and aortic dissection +8 more | |
| | | Single nucleotide variant (missense variant) | Marfan syndrome +8 more | |
| | | Single nucleotide variant (missense variant) | Familial thoracic aortic aneurysm and aortic dissection +9 more | |
| | | Single nucleotide variant (missense variant) | Familial thoracic aortic aneurysm and aortic dissection +9 more | |
| | | Single nucleotide variant (missense variant) | not specified +10 more | |
| | | Single nucleotide variant (missense variant) | Ectopia lentis 1, isolated, autosomal dominant +9 more | |
| | | Single nucleotide variant (missense variant) | Familial thoracic aortic aneurysm and aortic dissection +8 more | |
| | | Single nucleotide variant (missense variant) | Stiff skin syndrome +8 more | |
| | | Single nucleotide variant (missense variant) | Familial thoracic aortic aneurysm and aortic dissection +9 more | |
| | | Single nucleotide variant (missense variant) | Familial thoracic aortic aneurysm and aortic dissection +9 more | |
| | | Single nucleotide variant (missense variant) | Familial thoracic aortic aneurysm and aortic dissection +8 more | |
| | | Single nucleotide variant (missense variant) | Marfan syndrome +10 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Marfan syndrome +9 more | |
| | | Single nucleotide variant (missense variant) | Familial thoracic aortic aneurysm and aortic dissection +10 more | |
| | | Single nucleotide variant (missense variant) | Marfan syndrome +8 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Familial thoracic aortic aneurysm and aortic dissection +9 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | See cases +10 more | |
| | | Single nucleotide variant (missense variant) | MASS syndrome +8 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +8 more | |
| | | Single nucleotide variant (missense variant) | Ectopia lentis 1, isolated, autosomal dominant +9 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Marfan syndrome +8 more | |
| | | Single nucleotide variant (missense variant) | not provided +9 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Geleophysic dysplasia 2 +8 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Marfan syndrome +9 more | |
| | | Single nucleotide variant (missense variant) | Ectopia lentis 1, isolated, autosomal dominant +8 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Familial thoracic aortic aneurysm and aortic dissection +8 more | |
| | | Deletion (inframe_deletion) | Marfan syndrome +9 more | |
| | | Single nucleotide variant (missense variant) | Marfan syndrome +8 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Familial thoracic aortic aneurysm and aortic dissection +8 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Geleophysic dysplasia 2 +8 more | |
| | | Single nucleotide variant (missense variant) | Geleophysic dysplasia 2 +8 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Familial thoracic aortic aneurysm and aortic dissection +8 more | |
| | | Single nucleotide variant (missense variant) | Familial thoracic aortic aneurysm and aortic dissection +9 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Stiff skin syndrome +9 more | |
| | | Single nucleotide variant (missense variant) | Marfan syndrome +9 more | |
| | | Single nucleotide variant (missense variant) | Marfan syndrome +9 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Familial thoracic aortic aneurysm and aortic dissection +8 more | |
| | | Single nucleotide variant (missense variant) | Geleophysic dysplasia 2 +9 more | |
| | | Single nucleotide variant (missense variant) | Familial thoracic aortic aneurysm and aortic dissection +9 more | |
| | | Single nucleotide variant (missense variant) | Geleophysic dysplasia 2 +8 more | |