{{Rsnum
|rsid=121908800
|Chromosome=7
|Orientation=plus
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene=CFTR
|position=117504365
|Gene_s=CFTR
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A,C,G
|CHROM=7
|CLNACC=RCV000046370.2; RCV000046371.2
|CLNALLE=2; 3
|CLNDBN=Cystic fibrosis
|CLNHGVS=NC_000007.13:g.117144419T>C; NC_000007.13:g.117144419T>G
|CLNSIG=1
|Disease=Cystic fibrosis
|FwdALT=A,C,G
|FwdREF=T
|GENEINFO=CFTR:1080
|GENE_ID=1080
|GENE_NAME=CFTR
|REF=T
|RSPOS=117144419
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;PMC;OTHERKG;LSD;OM;NOV
|VC=SNV
|VP=0x050068000000000002110104
|WGT=0
|dbSNPBuildID=133
|rsid=121908800
|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=9482579
|Title=Detection of five novel mutations of the cystic fibrosis transmembrane regulator (CFTR) gene in Pakistani patients with cystic fibrosis: Y569D, Q98X, 296+12(T>C), 1161delC and 621+2(T>C).
}}