{{Rsnum
|rsid=121908778
|Chromosome=7
|Orientation=plus
|geno1=(-;-)
|geno2=(-;G)
|geno3=(G;G)
|Gene=CFTR
|position=117592078
|Gene_s=CFTR
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=121908778
|Reversed=0
|FwdREF=AG
|FwdALT=
A,AC
|REF=AG
|ALT=A,AC
|RSPOS=117232131
|CHROM=7
|dbSNPBuildID=136
|SSR=0
|SAO=1
|VP=0x050268000000000402110200
|GENEINFO=CFTR:1080
|GENE_NAME=CFTR
|GENE_ID=1080
|WGT=0
|VC=DIV
|CLNALLE=1
|CLNHGVS=NC_000007.13:g.117232132delG
|CLNSRC=Correlagen
|CLNORIGIN=1
|CLNSIG=5
|CLNDBN=Cystic fibrosis
|Disease=Cystic fibrosis
|Tags=PM;PMC;S3D;HD;OTHERKG;LSD;OM
|CLNACC=RCV000029489.2
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1250:C0010674:219700:586:190905008
}}{{PMID Auto
|PMID=1867536
|Title=Hepatic venous oxygen saturation monitoring in patients with assisted circulation for severe cardiac failure.
}}

{{PMID Auto
|PMID=12007216
|Title=Cystic fibrosis: a worldwide analysis of CFTR mutations--correlation with incidence data and application to screening.
}}

{{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=1284534
|Title=Mutations and sequence variations detected in the cystic fibrosis transmembrane conductance regulator (CFTR) gene: a report from the Cystic Fibrosis Genetic Analysis Consortium.
}}

{{PMID Auto
|PMID=7525450
|Title=Detection of more than 50 different CFTR mutations in a large group of German cystic fibrosis patients.
}}

{{PMID Auto
|PMID=9521595
|Title=Analysis of the CFTR gene in Turkish cystic fibrosis patients: identification of three novel mutations (3172delAC, P1013L and M1028I).
}}

{{PMID Auto
|PMID=12521276
|Title=Cystic fibrosis transmembrane regulator gene mutations in Bahrain.
}}

{{PMID Auto
|PMID=20797923
|Title=Mutational spectrum of cystic fibrosis in the Lebanese population.
}}
{{omim
|id=602421
|rsnum=121908778
}}