| | | Deletion (frameshift variant) | Ehlers-Danlos syndrome due to tenascin-X deficiency | |
| | LOC106780803, TNXB (T3993A +2 more) | Single nucleotide variant (missense variant) | Ehlers-Danlos syndrome due to tenascin-X deficiency | |
| | | Single nucleotide variant (missense variant) | Ehlers-Danlos syndrome due to tenascin-X deficiency | |
| | LOC106780803, TNXB (D4124N +2 more) | Single nucleotide variant (missense variant) | Ehlers-Danlos syndrome due to tenascin-X deficiency | |
| | | Single nucleotide variant (missense variant) | Ehlers-Danlos syndrome due to tenascin-X deficiency +1 more | |
| | | Single nucleotide variant (splice donor variant) | Ehlers-Danlos syndrome due to tenascin-X deficiency | |
| | | Single nucleotide variant (missense variant) | Ehlers-Danlos syndrome due to tenascin-X deficiency | |
| | | Deletion | Ehlers-Danlos syndrome due to tenascin-X deficiency | |
| | | Single nucleotide variant (missense variant) | Ehlers-Danlos syndrome due to tenascin-X deficiency +2 more | |
| | | Single nucleotide variant (missense variant) | Ehlers-Danlos syndrome due to tenascin-X deficiency +1 more | |
| | | Duplication (frameshift variant) | Vesicoureteral reflux 8 +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Ehlers-Danlos syndrome due to tenascin-X deficiency | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Ehlers-Danlos syndrome due to tenascin-X deficiency | |
| | LOC106780803, TNXB (R4052P +2 more) | Single nucleotide variant (missense variant) | Ehlers-Danlos syndrome due to tenascin-X deficiency | |
| | | Single nucleotide variant (missense variant) | Ehlers-Danlos syndrome due to tenascin-X deficiency | |
| | | Single nucleotide variant (missense variant) | Ehlers-Danlos syndrome due to tenascin-X deficiency | |
| | | Deletion (inframe_deletion) | Ehlers-Danlos syndrome due to tenascin-X deficiency | |
| | | Single nucleotide variant (missense variant) | Ehlers-Danlos syndrome due to tenascin-X deficiency | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Ehlers-Danlos syndrome due to tenascin-X deficiency | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +2 more | |
| | | Single nucleotide variant (intron variant) | not provided +2 more | |
| | | Single nucleotide variant (synonymous variant) | Vesicoureteral reflux 8 +2 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +2 more | |
| | | Single nucleotide variant (missense variant) | Vesicoureteral reflux 8 +1 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +2 more | |
| | | Single nucleotide variant (intron variant) | Vesicoureteral reflux 8 +1 more | |
| | | Single nucleotide variant (missense variant) | Ehlers-Danlos syndrome due to tenascin-X deficiency | |
| | | Single nucleotide variant (missense variant) | Vesicoureteral reflux 8 +2 more | |
| | LOC106780803, TNXB (N4174fs +2 more) | Duplication (frameshift variant) | Ehlers-Danlos syndrome due to tenascin-X deficiency | |
| | | Single nucleotide variant (missense variant) | not provided +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | Vesicoureteral reflux 8 +1 more | |
| | | Single nucleotide variant (missense variant) | Ehlers-Danlos syndrome +4 more | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Vesicoureteral reflux 8 +3 more | |
| | | Single nucleotide variant (splice donor variant) | Cardiovascular phenotype +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +1 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +1 more | |
| | | Deletion (inframe_deletion) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | Ehlers-Danlos syndrome due to tenascin-X deficiency | |
| | | Single nucleotide variant (missense variant) | Ehlers-Danlos syndrome +4 more | |
| | | Single nucleotide variant (missense variant) | Ehlers-Danlos syndrome +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Ehlers-Danlos syndrome +2 more | |
| | | Single nucleotide variant (missense variant) | Ehlers-Danlos syndrome due to tenascin-X deficiency +3 more | |
| | | Microsatellite (intron variant) | Ehlers-Danlos syndrome due to tenascin-X deficiency +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Ehlers-Danlos syndrome due to tenascin-X deficiency +2 more | |
| | | Single nucleotide variant (missense variant) | Ehlers-Danlos syndrome due to tenascin-X deficiency +4 more | |
| | | Single nucleotide variant (synonymous variant) | Vesicoureteral reflux 8 +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Ehlers-Danlos syndrome due to tenascin-X deficiency +4 more | |
| | | Single nucleotide variant (missense variant) | Ehlers-Danlos syndrome due to tenascin-X deficiency +4 more | |
| | | Single nucleotide variant (missense variant) | Ehlers-Danlos syndrome due to tenascin-X deficiency +4 more | |
| | | Single nucleotide variant (missense variant) | Ehlers-Danlos syndrome due to tenascin-X deficiency +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Ehlers-Danlos syndrome due to tenascin-X deficiency +3 more | |
| | | Single nucleotide variant (missense variant) | Ehlers-Danlos syndrome due to tenascin-X deficiency +4 more | |
| | | Single nucleotide variant (intron variant +1 more) | Vesicoureteral reflux 8 +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +3 more | |
| | | Single nucleotide variant (intron variant) | Ehlers-Danlos syndrome due to tenascin-X deficiency +2 more | |
| | | Single nucleotide variant (nonsense) | not provided +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Ehlers-Danlos syndrome due to tenascin-X deficiency +3 more | |
| | | Single nucleotide variant (missense variant) | Ehlers-Danlos syndrome +4 more | |
| | | Single nucleotide variant (missense variant) | Ehlers-Danlos syndrome due to tenascin-X deficiency +3 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +4 more | |
| | | Single nucleotide variant (missense variant) | TNXB-related condition +4 more | |
| | | Single nucleotide variant (missense variant) | Vesicoureteral reflux 8 +5 more | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | Ehlers-Danlos syndrome due to tenascin-X deficiency +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (nonsense) | not provided | |
| | LOC106780803, TNXB (A4196T +2 more) | Single nucleotide variant (missense variant) | Vesicoureteral reflux 8 +2 more | |
| | | Single nucleotide variant (missense variant) | not provided +3 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +3 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +3 more | |
| | | Single nucleotide variant (missense variant) | not provided +3 more | |
| | | Single nucleotide variant (intron variant) | not provided +2 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +3 more | |
| | | Single nucleotide variant (synonymous variant) | Vesicoureteral reflux 8 +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Ehlers-Danlos syndrome +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Ehlers-Danlos syndrome due to tenascin-X deficiency | |
| | | Single nucleotide variant (missense variant) | Ehlers-Danlos syndrome due to tenascin-X deficiency | |
| | | Single nucleotide variant (missense variant) | not provided +2 more | |
| | | Single nucleotide variant (missense variant) | Ehlers-Danlos syndrome due to tenascin-X deficiency | |
| | | Single nucleotide variant (missense variant) | not provided +2 more | |
| | | Deletion (frameshift variant) | Ehlers-Danlos syndrome due to tenascin-X deficiency | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +2 more | |
| | | Single nucleotide variant (missense variant) | Ehlers-Danlos syndrome due to tenascin-X deficiency +1 more | |
| | | Single nucleotide variant (missense variant) | Ehlers-Danlos syndrome due to tenascin-X deficiency | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +1 more | |
| | LOC106780803, TNXB (D172N +2 more) | Single nucleotide variant (missense variant) | Ehlers-Danlos syndrome due to tenascin-X deficiency +1 more | |
| | | Single nucleotide variant (missense variant) | not provided +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Vesicoureteral reflux 8 +4 more | |
| | | Single nucleotide variant (missense variant) | Ehlers-Danlos syndrome +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Vesicoureteral reflux 8 +3 more | |
| | | Single nucleotide variant (missense variant) | TNXB-related condition +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Ehlers-Danlos syndrome due to tenascin-X deficiency +3 more | |
| | | Single nucleotide variant (missense variant) | Ehlers-Danlos syndrome +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Ehlers-Danlos syndrome due to tenascin-X deficiency +1 more | |
| | LOC106780803, TNXB (P26S +2 more) | Single nucleotide variant (missense variant) | Ehlers-Danlos syndrome due to tenascin-X deficiency | |
| | | Single nucleotide variant (missense variant) | Ehlers-Danlos syndrome due to tenascin-X deficiency | |