{{Rsnum
|rsid=121908805
|Chromosome=7
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=CFTR
|position=117559468
|Gene_s=CFTR
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=121908805
|Reversed=0
|FwdREF=C
|FwdALT=A,G,T
|REF=C
|ALT=A,G,T
|RSPOS=117199522
|CHROM=7
|dbSNPBuildID=136
|SSR=0
|SAO=1
|VP=0x050268000000000002110104
|GENEINFO=CFTR:1080
|GENE_NAME=CFTR
|GENE_ID=1080
|WGT=0
|VC=SNV
|CLNALLE=1; 2; 3
|CLNHGVS=NC_000007.13:g.117199522C>A; NC_000007.13:g.117199522C>G; NC_000007.13:g.117199522C>T
|CLNSRC=CFTR2
|CLNORIGIN=1
|CLNSIG=5
|CLNCUI=
|CLNDBN=Cystic fibrosis
|Disease=Cystic fibrosis
|CLNACC=
RCV000056348.2; RCV000029475.3; RCV000046294.2
|Tags=PM;PMC;S3D;OTHERKG;LSD;OM;NOV
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1250:C0010674:219700:586:190905008
|CLNSRCID=S466X_67912; S466X_44486
}}{{PMID|2810954}} The histological assessment and evaluation of a 4 day subrenal capsule assay by the percentage inhibition of DNA/protein.

{{PMID|2810954}} The histological assessment and evaluation of a 4 day subrenal capsule assay by the percentage inhibition of DNA/protein.

{{PMID|7509683}} Three novel mutations (I506S, S466X, 1651A-->T) in exon 10 of the cystic fibrosis transmembrane conductance regulator (CFTR) detected in patients of southern German descent.
{{omim
|id=602421
|rsnum=121908805
}}