{{Rsnum
|rsid=121908793
|Chromosome=7
|Orientation=plus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=CFTR
|position=117535247
|Gene_s=CFTR
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=7
|CLNACC=RCV000056398.2
|CLNALLE=1
|CLNDBN=Cystic fibrosis
|CLNHGVS=NC_000007.13:g.117175301G>T
|CLNSIG=5
|Disease=Cystic fibrosis
|FwdALT=T
|FwdREF=G
|GENEINFO=CFTR:1080
|GENE_ID=1080
|GENE_NAME=CFTR
|REF=G
|RSPOS=117175301
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;PMC;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050068000000000002110100
|WGT=0
|dbSNPBuildID=133
|rsid=121908793
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1250:C0010674:219700:586:190905008
|CLNSRC=CFTR2
|CLNSRCID=712-1G->T
}}{{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=15371903
|Title=CFTR mutation distribution among U.S. Hispanic and African American individuals: evaluation in cystic fibrosis patient and carrier screening populations.
}}