{{Rsnum
|rsid=193922525
|Chromosome=7
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=CFTR
|position=117664770
|Gene_s=CFTR
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=193922525
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=117304824
|CHROM=7
|dbSNPBuildID=136
|SSR=0
|SAO=1
|VP=0x050268000000000002100100
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000007.13:g.117304824G>A
|CLNSRC=Correlagen
|CLNORIGIN=1
|CLNSIG=5
|CLNDBN=Cystic fibrosis
|Disease=Cystic fibrosis
|Tags=PM;PMC;S3D;OTHERKG;LSD
|CLNACC=RCV000029536.2
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1250:C0010674:219700:586:190905008
|GENEINFO=CFTR:1080
|GENE_ID=1080
|GENE_NAME=CFTR
}}{{PMID Auto
|PMID=995076
|Title=[The Wolff-Parkinson-White syndrome. Report of 3 cases and clinical considerations].
}}

{{PMID Auto
|PMID=9272157
|Title=Distinct spectrum of CFTR gene mutations in congenital absence of vas deferens.
}}

{{PMID Auto
|PMID=11242048
|Title=Aberrant CFTR-dependent HCO3- transport in mutations associated with cystic fibrosis.
|OA=1
}}

{{PMID Auto
|PMID=12124743
|Title=Genotype-phenotype correlation in cystic fibrosis: the role of modifier genes.
}}

{{PMID Auto
|PMID=17578899
|Title=Discovery of alpha-aminoazaheterocycle-methylglyoxal adducts as a new class of high-affinity inhibitors of cystic fibrosis transmembrane conductance regulator chloride channels.
}}

{{PMID Auto
|PMID=19114635
|Title=Mutations at the signature sequence of CFTR create a Cd(2+)-gated chloride channel.
|OA=1
}}