{{Rsnum
|rsid=76151804
|Chromosome=7
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=CFTR
|position=117611555
|Gene_s=CFTR
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=76151804
|Reversed=0
|FwdREF=A
|FwdALT=G
|REF=A
|ALT=G
|RSPOS=117251609
|CHROM=7
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050068000000000402110100
|GENEINFO=CFTR:1080
|GENE_NAME=CFTR
|GENE_ID=1080
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000007.13:g.117251609A>G
|CLNSRC=CFTR2
|CLNORIGIN=1
|CLNSIG=5
|CLNDBN=Cystic fibrosis
|Disease=Cystic fibrosis
|Tags=PM;PMC;HD;OTHERKG;LSD;OM
|CLNACC=RCV000029519.3
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1250:C0010674:219700:586:190905008
|CLNSRCID=3272-26A->G
}}{{PMID Auto
|PMID=1867536
|Title=Hepatic venous oxygen saturation monitoring in patients with assisted circulation for severe cardiac failure.
}}

{{PMID Auto
|PMID=2810954
|Title=The histological assessment and evaluation of a 4 day subrenal capsule assay by the percentage inhibition of DNA/protein.
}}

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

{{PMID Auto
|PMID=750841
|Title=Anthropometric estimation of body density, fat, and lean body weight in women gymnasts.
}}

{{PMID Auto
|PMID=1379210
|Title=Molecular characterization of cystic fibrosis: 16 novel mutations identified by analysis of the whole cystic fibrosis conductance transmembrane regulator (CFTR) coding regions and splice site junctions.
}}

{{PMID Auto
|PMID=11022925
|Title=Neonatal screening for cystic fibrosis in Brittany, France: assessment of 10 years' experience and impact on prenatal diagnosis.
}}

{{PMID Auto
|PMID=11168023
|Title=The molecular basis of cystic fibrosis in South Africa.
}}

{{PMID Auto
|PMID=12955726
|Title=CFTR genotypes in patients with normal or borderline sweat chloride levels.
}}

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