{{Rsnum
|rsid=121908791
|Chromosome=7
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=CFTR
|position=117509143
|Gene_s=CFTR
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=7
|CLNACC=RCV000056369.2
|CLNALLE=1
|CLNDBN=Cystic fibrosis
|CLNHGVS=NC_000007.13:g.117149197G>A
|CLNSIG=5
|Disease=Cystic fibrosis
|FwdALT=A
|FwdREF=G
|GENEINFO=CFTR:1080
|GENE_ID=1080
|GENE_NAME=CFTR
|REF=G
|RSPOS=117149197
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;PMC;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050068000000000002110100
|WGT=0
|dbSNPBuildID=133
|rsid=121908791
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1250:C0010674:219700:586:190905008
|CLNSRC=CFTR2
|CLNSRCID=405+1G->A
}}{{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=15948195
|Title=Mutation spectrum in Jewish cystic fibrosis patients in Israel: implication to carrier screening.
}}