| | | Single nucleotide variant (missense variant) | Congenital bilateral aplasia of vas deferens from CFTR mutation | |
| | | Single nucleotide variant (missense variant) | Congenital bilateral aplasia of vas deferens from CFTR mutation +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Congenital bilateral aplasia of vas deferens from CFTR mutation | |
| | | Single nucleotide variant (missense variant) | Cystic fibrosis +1 more | |
| | | Single nucleotide variant (missense variant) | not provided +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Cystic fibrosis +3 more | |
| | | Single nucleotide variant (nonsense +1 more) | Cystic fibrosis | |
| | | Single nucleotide variant (missense variant) | Congenital bilateral aplasia of vas deferens from CFTR mutation +1 more | |
| | | Single nucleotide variant (missense variant) | Congenital bilateral aplasia of vas deferens from CFTR mutation +1 more | |
| | | Single nucleotide variant (missense variant) | Congenital bilateral aplasia of vas deferens from CFTR mutation +1 more | |
| | | Single nucleotide variant (missense variant) | not specified +2 more | |
| | | Single nucleotide variant (missense variant) | Cystic fibrosis +2 more | |
| | | Deletion (intron variant) | Cystic fibrosis +6 more | |
| | | Single nucleotide variant (intron variant) | Congenital bilateral aplasia of vas deferens from CFTR mutation | |
| | | Single nucleotide variant (missense variant) | Congenital bilateral aplasia of vas deferens from CFTR mutation +1 more | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | Cystic fibrosis +4 more | |
| | | Single nucleotide variant (missense variant) | not specified +4 more | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (3 prime UTR variant) | Bronchiectasis with or without elevated sweat chloride 1 +4 more | |
| | | Single nucleotide variant (synonymous variant) | Cystic fibrosis +2 more | GConflicting classifications of pathogenicity |
| | CFTR, CFTR-AS1 (G576A +2 more) | Single nucleotide variant (missense variant) | Cystic fibrosis | |
| | CFTR, LOC111674472 (M1101I) | Single nucleotide variant (missense variant) | Bronchiectasis with or without elevated sweat chloride 1 +3 more | |
| | | Single nucleotide variant (missense variant) | Bronchiectasis with or without elevated sweat chloride 1 +3 more | |
| | | Single nucleotide variant (missense variant) | Cystic fibrosis +5 more | |
| | | Deletion (intron variant) | Cystic fibrosis +4 more | |
| | | Microsatellite (intron variant) | Cystic fibrosis | |
| | | Single nucleotide variant (nonsense) | Cystic fibrosis +2 more | GPathogenic/Likely pathogenic |
| | | Duplication (frameshift variant) | Cystic fibrosis +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (nonsense) | Cystic fibrosis +1 more | GPathogenic/Likely pathogenic |
| | LOC113664106, CFTR (E60fs) | Microsatellite (frameshift variant) | Cystic fibrosis +1 more | |
| | | Single nucleotide variant (missense variant) | not provided +6 more | |
| | | Single nucleotide variant (missense variant) | Bronchiectasis with or without elevated sweat chloride 1 +6 more | |
| | LOC111674472, CFTR (F1107L) | Single nucleotide variant (missense variant) | Cystic fibrosis +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Deletion (splice acceptor variant +1 more) | Congenital bilateral aplasia of vas deferens from CFTR mutation | |
| | | Deletion (frameshift variant) | Congenital bilateral aplasia of vas deferens from CFTR mutation | |
| | | Deletion (frameshift variant) | Congenital bilateral aplasia of vas deferens from CFTR mutation | |
| | | Single nucleotide variant (nonsense) | Congenital bilateral aplasia of vas deferens from CFTR mutation | |
| | | Duplication (frameshift variant) | Congenital bilateral aplasia of vas deferens from CFTR mutation | |
| | | Single nucleotide variant (nonsense) | Congenital bilateral aplasia of vas deferens from CFTR mutation | |
| | | Indel (missense variant) | Congenital bilateral aplasia of vas deferens from CFTR mutation +4 more | GConflicting classifications of pathogenicity |
| | | Deletion (inframe_deletion +1 more) | Cystic fibrosis | |
| | CFTR, CFTR-AS1 +1 more (S466* +1 more) | Single nucleotide variant (nonsense +1 more) | Cystic fibrosis | |
| | | Single nucleotide variant (missense variant) | Bronchiectasis with or without elevated sweat chloride 1 +6 more | |
| | | Single nucleotide variant (missense variant) | Bronchiectasis with or without elevated sweat chloride 1 +3 more | GConflicting classifications of pathogenicity |
| | LOC111674472, CFTR (T1036I) | Single nucleotide variant (missense variant) | Bronchiectasis with or without elevated sweat chloride 1 +2 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (nonsense) | Cystic fibrosis +1 more | |
| | CFTR, LOC111674472 (W1098C) | Single nucleotide variant (missense variant) | Cystic fibrosis | |
| | | Single nucleotide variant (missense variant) | not provided +4 more | |
| | CFTR, LOC111674475 (I539T) | Single nucleotide variant (missense variant) | not provided +5 more | |
| | | Single nucleotide variant (missense variant) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Hereditary pancreatitis +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +3 more | |
| | | Single nucleotide variant (missense variant) | Hereditary pancreatitis +5 more | |
| | | Single nucleotide variant (missense variant) | Hereditary pancreatitis +5 more | |
| | | Single nucleotide variant (missense variant) | Hereditary pancreatitis +4 more | |
| | CFTR, LOC111674477 (E1433*) | Single nucleotide variant (nonsense) | Bronchiectasis with or without elevated sweat chloride 1 +2 more | GPathogenic/Likely pathogenic |
| | | Microsatellite (frameshift variant) | Cystic fibrosis +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (splice donor variant) | Hereditary pancreatitis +4 more | GPathogenic/Likely pathogenic |
| | | Deletion (frameshift variant) | Cystic fibrosis | |
| | | Single nucleotide variant (missense variant) | Congenital bilateral aplasia of vas deferens from CFTR mutation +5 more | |
| | | Single nucleotide variant (splice acceptor variant) | Cystic fibrosis +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | not specified +4 more | |
| | | Single nucleotide variant (splice acceptor variant) | Cystic fibrosis +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not specified +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +5 more | |
| | | Single nucleotide variant (missense variant) | not provided +5 more | |
| | | Single nucleotide variant (missense variant) | not specified +4 more | |
| | | Single nucleotide variant (missense variant) | Cystic fibrosis +4 more | |
| | | Single nucleotide variant | Cystic fibrosis +4 more | |
| | | Single nucleotide variant (missense variant) | Cystic fibrosis +5 more | |
| | | Single nucleotide variant (missense variant) | not provided +4 more | |
| | | Single nucleotide variant (missense variant) | Cystic fibrosis +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Cystic fibrosis | |
| | | Single nucleotide variant (missense variant) | Cystic fibrosis +5 more | |
| | CFTR, LOC111674472 (Y1092H) | Single nucleotide variant (missense variant) | not specified +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Cystic fibrosis +6 more | |
| | CFTR, LOC111674472 (I1051V) | Single nucleotide variant (missense variant) | Cystic fibrosis +5 more | |
| | | Single nucleotide variant (missense variant) | not provided +4 more | |
| | | Single nucleotide variant (missense variant) | not provided +4 more | |
| | | Single nucleotide variant (missense variant) | not provided +4 more | |
| | | Single nucleotide variant (missense variant) | not specified +4 more | |
| | | Single nucleotide variant (missense variant) | Cystic fibrosis +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Cystic fibrosis +4 more | |
| | | Single nucleotide variant (missense variant) | not specified +6 more | |
| | | Single nucleotide variant (nonsense) | Cystic fibrosis +1 more | GPathogenic/Likely pathogenic |
| | | Microsatellite (frameshift variant) | Cystic fibrosis | |
| | | Single nucleotide variant (missense variant) | not specified +5 more | |
| | | Single nucleotide variant (missense variant) | Cystic fibrosis +4 more | |
| | | Single nucleotide variant (missense variant) | Cystic fibrosis +5 more | |
| | | Single nucleotide variant (missense variant) | not specified +5 more | |
| | | Single nucleotide variant (missense variant) | Cystic fibrosis +6 more | |
| | | Indel | not provided +2 more | GPathogenic/Likely pathogenic |
| | | Deletion (frameshift variant) | Congenital bilateral aplasia of vas deferens from CFTR mutation +3 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (intron variant) | not specified +3 more | GConflicting classifications of pathogenicity |
| | CFTR, LOC111674472 (T1086S) | Single nucleotide variant (missense variant) | not provided +4 more | |
| | | Single nucleotide variant (missense variant) | Congenital bilateral aplasia of vas deferens from CFTR mutation +4 more | |
| | | Single nucleotide variant (missense variant) | CFTR-related disorder +6 more | |
| | | Single nucleotide variant (missense variant) | Congenital bilateral aplasia of vas deferens from CFTR mutation +5 more | |