| | | Single nucleotide variant (3 prime UTR variant +1 more) | TERT-related disorder | |
| | | Single nucleotide variant (missense variant +1 more) | Dyskeratosis congenita, autosomal dominant 2 +3 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Idiopathic Pulmonary Fibrosis +3 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 +6 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Dyskeratosis congenita +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +1 more) | Dyskeratosis congenita +3 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | not specified +4 more | |
| | | Single nucleotide variant (missense variant +1 more) | Dyskeratosis congenita +7 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +1 more) | not specified +4 more | |
| | | Single nucleotide variant (intron variant) | Idiopathic Pulmonary Fibrosis +2 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | TERT-related disorder +3 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Idiopathic Pulmonary Fibrosis +4 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Dyskeratosis congenita +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | TERT-related disorder +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +1 more) | Dyskeratosis congenita +3 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Pulmonary fibrosis and/or bone marrow failure, Telomere-related, 1 +7 more | |
| | | Single nucleotide variant (intron variant) | Idiopathic Pulmonary Fibrosis +2 more | |
| | | Single nucleotide variant (intron variant) | not specified +3 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | TERT-related disorder +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +1 more) | Dyskeratosis congenita +3 more | |
| | | Single nucleotide variant (intron variant) | Idiopathic Pulmonary Fibrosis +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +1 more) | Dyskeratosis congenita +5 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Idiopathic Pulmonary Fibrosis +2 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 +3 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Dyskeratosis congenita +6 more | |
| | | Single nucleotide variant (missense variant +1 more) | Dyskeratosis congenita, autosomal dominant 2 +2 more | |
| | | Single nucleotide variant (missense variant +1 more) | TERT-related disorder +2 more | GConflicting classifications of pathogenicity |
| | | Duplication (intron variant +1 more) | Pulmonary fibrosis and/or bone marrow failure, Telomere-related, 1 +3 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided +5 more | |
| | | Single nucleotide variant (intron variant) | Dyskeratosis congenita, autosomal dominant 2 +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Dyskeratosis congenita, autosomal dominant 2 +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | Idiopathic Pulmonary Fibrosis +2 more | |
| | | Single nucleotide variant (missense variant +1 more) | TERT-related disorder | |
| | | Single nucleotide variant (synonymous variant +1 more) | Pulmonary fibrosis and/or bone marrow failure, Telomere-related, 1 +5 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided +7 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Dyskeratosis congenita +3 more | |
| | | Single nucleotide variant (missense variant) | Dyskeratosis congenita +1 more | |
| | | Single nucleotide variant (intron variant) | not provided +10 more | |
| | | Single nucleotide variant (intron variant) | Dyskeratosis congenita, autosomal dominant 2 +2 more | |
| | | Single nucleotide variant (intron variant) | not specified +2 more | |
| | | Single nucleotide variant (intron variant) | Dyskeratosis congenita, autosomal dominant 2 +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Dyskeratosis congenita +4 more | |
| | | Single nucleotide variant (synonymous variant) | not specified +4 more | |
| | | Single nucleotide variant (synonymous variant) | Dyskeratosis congenita, autosomal dominant 2 +4 more | |
| | | Single nucleotide variant (missense variant) | TERT-related disorder +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | TERT-related disorder +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | not specified +10 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +1 more) | TERT-related disorder +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +1 more) | Dyskeratosis congenita +3 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Dyskeratosis congenita, autosomal dominant 2 +4 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | not specified +4 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Idiopathic Pulmonary Fibrosis +3 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Dyskeratosis congenita +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | not provided +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +1 more) | Idiopathic Pulmonary Fibrosis +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +1 more) | Dyskeratosis congenita +3 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Idiopathic Pulmonary Fibrosis +5 more | |
| | | Single nucleotide variant (intron variant) | Dyskeratosis congenita, autosomal dominant 2 +7 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Idiopathic Pulmonary Fibrosis +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +1 more) | Dyskeratosis congenita, autosomal dominant 2 +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +1 more) | Idiopathic Pulmonary Fibrosis +7 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Dyskeratosis congenita, autosomal dominant 2 +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | Dyskeratosis congenita +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +1 more) | Dyskeratosis congenita +9 more | |
| | | Single nucleotide variant (missense variant +1 more) | TERT-related disorder +3 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Acute myeloid leukemia +7 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +3 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Idiopathic Pulmonary Fibrosis +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +1 more) | TERT-related disorder +3 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Dyskeratosis congenita, autosomal dominant 2 +7 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +1 more) | not specified +4 more | |
| | | Single nucleotide variant (intron variant) | Pulmonary fibrosis and/or bone marrow failure, Telomere-related, 1 +6 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Dyskeratosis congenita, autosomal dominant 2 +10 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +13 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +1 more) | TERT-related disorder +3 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Pulmonary fibrosis and/or bone marrow failure, Telomere-related, 1 +7 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +1 more) | Dyskeratosis congenita +3 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Dyskeratosis congenita +5 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Pulmonary fibrosis and/or bone marrow failure, Telomere-related, 1 +6 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Dyskeratosis congenita +3 more | |
| | | Single nucleotide variant (intron variant) | not specified +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +1 more) | TERT-related disorder +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | TERT-related disorder +3 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Dyskeratosis congenita, autosomal dominant 2 +7 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Idiopathic Pulmonary Fibrosis +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | TERT-related disorder | |
| | | Single nucleotide variant (synonymous variant +1 more) | Dyskeratosis congenita +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | Dyskeratosis congenita, autosomal dominant 2 +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Idiopathic Pulmonary Fibrosis +9 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | not provided +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | TERT-related disorder +3 more | GConflicting classifications of pathogenicity |
| | | Microsatellite (inframe_deletion +1 more) | Dyskeratosis congenita +11 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +1 more) | Dyskeratosis congenita +3 more | |
| | | Deletion (frameshift variant +1 more) | TERT-related disorder +2 more | |
| | | Single nucleotide variant (missense variant +1 more) | not specified +9 more | |
| | | Single nucleotide variant (missense variant +1 more) | Dyskeratosis congenita +3 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Dyskeratosis congenita +3 more | |