{{Rsnum
|rsid=121908757
|Chromosome=7
|Orientation=plus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=CFTR
|position=117587799
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CFTR
}}{{omim
|id=602421
|rsnum=121908757
|variant=0012
}}{{ClinVar
|rsid=121908757
|Reversed=0
|FwdREF=A
|FwdALT=C
|REF=A
|ALT=C
|RSPOS=117227853
|CHROM=7
|dbSNPBuildID=133
|SSR=0
|SAO=0
|VP=0x050268000000000002110100
|GENEINFO=CFTR:1080
|GENE_NAME=CFTR
|GENE_ID=1080
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000007.13:g.117227853A>C
|CLNSRC=CFTR2; Cystic Fibrosis Mutation Database; GTR
|CLNSRCID=S549R_47338; 261; GTR000257096; GTR000500233
|CLNSIG=5
|CLNCUI=C0010674; C0010674; C0010674
|CLNDBN=Cystic fibrosis
|Disease=Cystic fibrosis
|CLNACC=RCV000007538.1; RCV000043664.2
|Tags=PM;PMC;S3D;OTHERKG;LSD;OM
|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=15948195
|Title=Mutation spectrum in Jewish cystic fibrosis patients in Israel: implication to carrier screening.
}}