{{Rsnum
|rsid=193922511
|Chromosome=7
|Orientation=plus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=CFTR
|position=117603687
|Gene_s=CFTR
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=193922511
|Reversed=0
|FwdREF=T
|FwdALT=G
|REF=T
|ALT=G
|RSPOS=117243741
|CHROM=7
|dbSNPBuildID=136
|SSR=0
|SAO=1
|VP=0x050068000000000002100100
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000007.13:g.117243741T>G
|CLNSRC=Correlagen
|CLNORIGIN=1
|CLNSIG=4
|CLNDBN=Congenital bilateral absence of the vas deferens; Cystic fibrosis
|Disease=Congenital bilateral absence of the vas deferens; Cystic fibrosis
|Tags=PM;PMC;OTHERKG;LSD
|CLNACC=RCV000029505.1; RCV000046693.2
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet; GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1250:CN032726:277180:48; NBK1250:C0010674:219700:586:190905008
|GENEINFO=CFTR:1080
|GENE_ID=1080
|GENE_NAME=CFTR
}}{{PMID Auto
|PMID=92721
|Title=Diatoms in lung tissue.
}}

{{PMID Auto
|PMID=10755189
|Title=CFTR gene mutations and male infertility.
}}

{{PMID Auto
|PMID=17175965
|Title=[Role of deep seminal tract imaging in the diagnosis of unilateral agenesis of the vas deferens. Case report of a patient with CFTR gene mutation].
}}

{{PMID Auto
|PMID=17329263
|Title=Detection of cystic fibrosis transmembrane conductance regulator (CFTR) gene rearrangements enriches the mutation spectrum in congenital bilateral absence of the vas deferens and impacts on genetic counselling.
}}

{{PMID Auto
|PMID=17507277
|Title=[Unilateral partial deferential agenesia and CFTR gene composite heterozygoty (deltaF508/V938G)].
}}

{{PMID Auto
|PMID=20059485
|Title=Do common in silico tools predict the clinical consequences of amino-acid substitutions in the CFTR gene?
}}