{{Rsnum
|rsid=121908747
|Chromosome=7
|Orientation=plus
|geno1=(-;-)
|geno2=(-;C)
|geno3=(C;C)
|Gene=CFTR
|position=117627581
|Gene_s=CFTR
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=121908747
|Reversed=0
|FwdREF=C
|FwdALT=
|REF=AC
|ALT=A
|RSPOS=117267633
|CHROM=7
|dbSNPBuildID=136
|SSR=0
|SAO=1
|VP=0x050068000000000002110200
|GENEINFO=CFTR:1080
|GENE_NAME=CFTR
|GENE_ID=1080
|WGT=0
|VC=DIV
|CLNALLE=1
|CLNHGVS=NC_000007.13:g.117267635delC
|CLNSRC=CFTR2; GTR
|CLNORIGIN=1
|CLNSRCID=3659delC; GTR000500233
|CLNSIG=5
|CLNCUI=C0010674
|CLNDBN=Cystic fibrosis
|Disease=Cystic fibrosis
|CLNACC=RCV000029523.4
|Tags=PM;PMC;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1250:C0010674:219700:586:190905008
}}{{PMID Auto
|PMID=11388756
|Title=Improved detection of cystic fibrosis mutations in the heterogeneous U.S. population using an expanded, pan-ethnic mutation panel.
}}

{{PMID Auto
|PMID=137921
|Title=Double-blind study of ipratropium bromide, a new anticholinergic bronchodilator.
}}

{{PMID Auto
|PMID=8889582
|Title=Fluorescent multiplex microsatellites used to define haplotypes associated with 75 CFTR mutations from the UK on 437 CF chromosomes.
}}

{{PMID Auto
|PMID=10636451
|Title=Three common CFTR mutations should be included in a neonatal screening programme for cystic fibrosis in Sweden.
}}

{{PMID Auto
|PMID=12865275
|Title=Molecular consequences of cystic fibrosis transmembrane regulator (CFTR) gene mutations in the exocrine pancreas.
|OA=1
}}

{{PMID Auto
|PMID=15371903
|Title=CFTR mutation distribution among U.S. Hispanic and African American individuals: evaluation in cystic fibrosis patient and carrier screening populations.
}}

{{PMID Auto
|PMID=16051530
|Title=Spectrum of mutations in CFTR in Finland: 18 years follow-up study and identification of two novel mutations.
}}