| | | Single nucleotide variant (5 prime UTR variant +2 more) | Ehlers-Danlos syndrome, periodontal type 2 | |
| | | Single nucleotide variant (missense variant) | Ehlers-Danlos syndrome, periodontal type 2 | |
| | | Single nucleotide variant (missense variant) | Ehlers-Danlos syndrome, periodontal type 2 | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | Ehlers-Danlos syndrome, periodontal type 2 | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided +2 more | |
| | | Single nucleotide variant (synonymous variant) | Ehlers-Danlos syndrome, periodontal type 2 +2 more | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | not provided | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Complement component C1s deficiency +2 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +2 more | |
| | | Single nucleotide variant (missense variant) | not provided +3 more | |
| | | Single nucleotide variant (missense variant) | Complement component C1s deficiency +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Ehlers-Danlos syndrome, periodontal type 2 +2 more | |
| | | Single nucleotide variant (missense variant) | Ehlers-Danlos syndrome, periodontal type 1 | |
| | | Indel (inframe_indel) | Ehlers-Danlos syndrome, periodontal type 1 | |
| | | Single nucleotide variant (missense variant) | Ehlers-Danlos syndrome, periodontal type 1 | |
| | | Single nucleotide variant (missense variant) | Ehlers-Danlos syndrome, periodontal type 1 | |
| | | Single nucleotide variant (missense variant) | Ehlers-Danlos syndrome, periodontal type 1 | |
| | | Single nucleotide variant (missense variant) | Ehlers-Danlos syndrome, periodontal type 1 | |
| | | Indel (missense variant) | Ehlers-Danlos syndrome, periodontal type 1 | |
| | | Single nucleotide variant (missense variant) | Ehlers-Danlos syndrome, periodontal type 1 | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Ehlers-Danlos syndrome, periodontal type 1 | |
| | | Indel (inframe_indel) | Ehlers-Danlos syndrome, periodontal type 1 | |
| | | Single nucleotide variant (missense variant) | Ehlers-Danlos syndrome, periodontal type 1 | |
| | | Single nucleotide variant (missense variant) | Ehlers-Danlos syndrome, periodontal type 1 | |
| | | Single nucleotide variant (missense variant) | Ehlers-Danlos syndrome, periodontal type 1 | |
| | | Single nucleotide variant (missense variant) | Ehlers-Danlos syndrome, periodontal type 1 | |
| | | Single nucleotide variant (missense variant) | Ehlers-Danlos syndrome, periodontal type 1 | |
| | | Deletion (inframe_indel) | Ehlers-Danlos syndrome, periodontal type 1 | |
| | | Single nucleotide variant (missense variant) | not provided +2 more | |