{{Rsnum
|rsid=121908811
|Chromosome=7
|Orientation=plus
|geno1=(-;-)
|geno2=(-;C)
|geno3=(C;C)
|Gene=CFTR
|position=117627712
|Gene_s=CFTR
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=7
|CLNACC=RCV000007544.3
|CLNALLE=1
|CLNDBN=Cystic fibrosis
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1250:C0010674:219700:586:190905008
|CLNHGVS=NC_000007.13:g.117267766delC
|CLNSIG=5
|CLNSRC=CFTR2; Cystic Fibrosis Mutation Database; GTR; OMIM Allelic Variant
|CLNSRCID=3791delC; 510; GTR000074114; GTR000257096; 602421.0020
|Disease=Cystic fibrosis
|FwdREF=C
|GENEINFO=CFTR:1080
|GENE_ID=1080
|GENE_NAME=CFTR
|REF=AC
|RSPOS=117267765
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;PMC;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050068000000000002110200
|WGT=0
|dbSNPBuildID=133
|rsid=121908811
}}{{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=15371903
|Title=CFTR mutation distribution among U.S. Hispanic and African American individuals: evaluation in cystic fibrosis patient and carrier screening populations.
}}