| | | Single nucleotide variant (3 prime UTR variant +1 more) | Dyskeratosis congenita, autosomal dominant 2 +2 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Pulmonary fibrosis and/or bone marrow failure, Telomere-related, 1 +2 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Aplastic anemia +2 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Dyskeratosis congenita, autosomal dominant 2 +2 more | |
| | | Deletion (3 prime UTR variant +1 more) | Interstitial lung disease 2 | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Pulmonary fibrosis and/or bone marrow failure, Telomere-related, 1 +2 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Pulmonary fibrosis and/or bone marrow failure, Telomere-related, 1 +2 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | not specified +4 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Pulmonary fibrosis and/or bone marrow failure, Telomere-related, 1 +2 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Pulmonary fibrosis and/or bone marrow failure, Telomere-related, 1 +2 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | not provided +3 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | TERT-related disorder | |
| | | Duplication | Dyskeratosis congenita, autosomal dominant 2 +1 more | |
| | | Duplication | Interstitial lung disease 2 +1 more | |
| | | Duplication | Interstitial lung disease 2 +1 more | |
| | | Duplication | Interstitial lung disease 2 +1 more | |
| | | Duplication | Dyskeratosis congenita, autosomal dominant 2 +1 more | |
| | | Single nucleotide variant (stop lost +1 more) | Pulmonary fibrosis and/or bone marrow failure, Telomere-related, 1 | |
| | | Single nucleotide variant (synonymous variant +1 more) | Idiopathic Pulmonary Fibrosis +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Dyskeratosis congenita, autosomal dominant 2 +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Hereditary cancer-predisposing syndrome +3 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Idiopathic Pulmonary Fibrosis +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Dyskeratosis congenita, autosomal dominant 2 +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Dyskeratosis congenita +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Dyskeratosis congenita +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +1 more) | Idiopathic Pulmonary Fibrosis +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | Idiopathic Pulmonary Fibrosis +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Hereditary cancer-predisposing syndrome +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | Dyskeratosis congenita, autosomal dominant 2 +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Hereditary cancer-predisposing syndrome +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | Dyskeratosis congenita, autosomal dominant 2 +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +2 more | |
| | | Single nucleotide variant (missense variant +1 more) | Dyskeratosis congenita, autosomal dominant 2 +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Idiopathic Pulmonary Fibrosis +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Idiopathic Pulmonary Fibrosis +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | TERT-related disorder +2 more | |
| | | Single nucleotide variant (missense variant +1 more) | Dyskeratosis congenita, autosomal dominant 2 +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Dyskeratosis congenita, autosomal dominant 2 +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | Idiopathic Pulmonary Fibrosis +3 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Dyskeratosis congenita +4 more | |
| | | Single nucleotide variant (missense variant +1 more) | Idiopathic Pulmonary Fibrosis +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Dyskeratosis congenita, autosomal dominant 2 +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Hereditary cancer-predisposing syndrome +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | Dyskeratosis congenita, autosomal dominant 2 +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Dyskeratosis congenita, autosomal dominant 2 +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Idiopathic Pulmonary Fibrosis +3 more | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Idiopathic Pulmonary Fibrosis +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Dyskeratosis congenita, autosomal dominant 2 +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Hereditary cancer-predisposing syndrome +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | Dyskeratosis congenita, autosomal dominant 2 +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Idiopathic Pulmonary Fibrosis +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Dyskeratosis congenita, autosomal dominant 2 +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Dyskeratosis congenita, autosomal dominant 2 +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Dyskeratosis congenita, autosomal dominant 2 +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Idiopathic Pulmonary Fibrosis +2 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Idiopathic Pulmonary Fibrosis +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Dyskeratosis congenita +7 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Idiopathic Pulmonary Fibrosis +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Hereditary breast ovarian cancer syndrome +2 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Dyskeratosis congenita +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +8 more | |
| | | Single nucleotide variant (missense variant +1 more) | Hereditary cancer-predisposing syndrome +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Hereditary cancer-predisposing syndrome +4 more | |
| | | Single nucleotide variant (missense variant +1 more) | Idiopathic Pulmonary Fibrosis +1 more | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Idiopathic Pulmonary Fibrosis +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Interstitial lung disease 2 +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Hereditary cancer-predisposing syndrome +7 more | |
| | | Single nucleotide variant (missense variant +1 more) | Hereditary cancer-predisposing syndrome +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | Dyskeratosis congenita, autosomal dominant 2 +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Idiopathic Pulmonary Fibrosis +3 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Dyskeratosis congenita, autosomal dominant 2 +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Idiopathic Pulmonary Fibrosis +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | Dyskeratosis congenita +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Dyskeratosis congenita, autosomal dominant 2 +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Idiopathic Pulmonary Fibrosis +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Dyskeratosis congenita, autosomal dominant 2 +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Dyskeratosis congenita, autosomal dominant 2 +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Dyskeratosis congenita, autosomal dominant 2 +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided +2 more | |
| | | Single nucleotide variant (missense variant +1 more) | Dyskeratosis congenita, autosomal dominant 2 +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Idiopathic Pulmonary Fibrosis +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Dyskeratosis congenita, autosomal dominant 2 +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Idiopathic Pulmonary Fibrosis +4 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided +10 more | |
| | | Single nucleotide variant (missense variant +1 more) | Dyskeratosis congenita, autosomal dominant 2 +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +1 more) | Idiopathic Pulmonary Fibrosis +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided | |
| | | Single nucleotide variant (missense variant +1 more) | Dyskeratosis congenita, autosomal dominant 2 +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Dyskeratosis congenita +1 more | |
| | | Single nucleotide variant (intron variant) | Dyskeratosis congenita, autosomal dominant 2 +1 more | |
| | | Single nucleotide variant (intron variant) | Idiopathic Pulmonary Fibrosis +1 more | |
| | | Single nucleotide variant (intron variant) | Dyskeratosis congenita, autosomal dominant 2 +1 more | |
| | | Single nucleotide variant (intron variant) | Idiopathic Pulmonary Fibrosis +1 more | |
| | | Single nucleotide variant (intron variant) | Idiopathic Pulmonary Fibrosis +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Interstitial lung disease 2 +1 more | |
| | | Single nucleotide variant (intron variant) | Dyskeratosis congenita, autosomal dominant 2 +1 more | |
| | | Single nucleotide variant (intron variant) | Dyskeratosis congenita, autosomal dominant 2 +1 more | |
| | | Single nucleotide variant (intron variant) | Dyskeratosis congenita, autosomal dominant 2 +1 more | |
| | | Single nucleotide variant (intron variant) | Idiopathic Pulmonary Fibrosis +1 more | |
| | | Single nucleotide variant (intron variant) | Idiopathic Pulmonary Fibrosis +1 more | |