{{Rsnum
|rsid=77834169
|Chromosome=7
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=CFTR
|position=117530974
|Gene_s=CFTR
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=G,T
|CHROM=7
|CLNACC=RCV000046914.2; RCV000056382.2
|CLNALLE=1; 2
|CLNDBN=Cystic fibrosis
|CLNHGVS=NC_000007.13:g.117171028C>G; NC_000007.13:g.117171028C>T
|CLNSIG=5
|CLNSRC=CFTR2; GTR
|CLNSRCID=R117C; GTR000074114
|Disease=Cystic fibrosis
|FwdALT=G,T
|FwdREF=C
|GENEINFO=CFTR:1080
|GENE_ID=1080
|GENE_NAME=CFTR
|REF=C
|RSPOS=117171028
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;PMC;HD;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050068000000000402110100
|WGT=0
|dbSNPBuildID=131
|rsid=77834169
|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=11491164
|Title=Intron-8 polythymidine sequence in Australasian individuals with CF mutations R117H and R117C.
}}

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