Links from MedGen
Items: 11
| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | | Deletion (frameshift variant +2 more) | Aortic aneurysm, familial thoracic 9 | |
| | | Single nucleotide variant (intron variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant +2 more) | Aortic aneurysm, familial thoracic 9 +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +2 more) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +2 more) | not provided +3 more | |
| | | Single nucleotide variant (missense variant +2 more) | not provided +2 more | |
| | | Single nucleotide variant (intron variant) | Aortic aneurysm, familial thoracic 9 +2 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Aortic aneurysm, familial thoracic 9 +3 more | |
| | | Single nucleotide variant (intron variant) | Cardiovascular phenotype +3 more | |
| | | Single nucleotide variant (missense variant +2 more) | not specified +1 more | GConflicting classifications of pathogenicity |
| | LOC126861443, MFAP5 (R158* +4 more) | Single nucleotide variant (nonsense +1 more) | Aortic aneurysm, familial thoracic 9 +2 more | GConflicting classifications of pathogenicity |
Click to view in NCBI Gene