{{Rsnum
|rsid=79031340
|Chromosome=7
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=CFTR
|position=117540218
|Gene_s=CFTR
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=7
|CLNACC=RCV000056402.2
|CLNALLE=1
|CLNDBN=Cystic fibrosis
|CLNHGVS=NC_000007.13:g.117180272G>T
|CLNSIG=5
|CLNSRC=CFTR2; GTR
|CLNSRCID=G330X; GTR000074114
|Disease=Cystic fibrosis
|FwdALT=T
|FwdREF=G
|GENEINFO=CFTR:1080
|GENE_ID=1080
|GENE_NAME=CFTR
|REF=G
|RSPOS=117180272
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;PMC;HD;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050068000000000402110100
|WGT=0
|dbSNPBuildID=131
|rsid=79031340
|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=11388756
|Title=Improved detection of cystic fibrosis mutations in the heterogeneous U.S. population using an expanded, pan-ethnic mutation panel.
}}

{{PMID Auto
|PMID=15371902
|Title=Cystic fibrosis population carrier screening: 2004 revision of American College of Medical Genetics mutation panel.
|OA=1
}}

{{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.
}}