{{Rsnum
|rsid=78756941
|Chromosome=7
|Orientation=plus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=CFTR
|position=117531115
|Gene_s=CFTR
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=7
|CLNACC=RCV000043565.3
|CLNALLE=1
|CLNDBN=Cystic fibrosis
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1250:C0010674:219700:586:190905008
|CLNHGVS=NC_000007.13:g.117171169G>T
|CLNSIG=5
|CLNSRC=CFTR2; Cystic Fibrosis Mutation Database; GTR
|CLNSRCID=621+1G->T; 112; GTR000074114; GTR000257096; GTR000500233
|Disease=Cystic fibrosis
|FwdALT=T
|FwdREF=G
|GENEINFO=CFTR:1080
|GENE_ID=1080
|GENE_NAME=CFTR
|REF=G
|RSPOS=117171169
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;PMC;HD;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050068000000000402110100
|WGT=0
|dbSNPBuildID=131
|rsid=78756941
}}{{PMID Auto
|PMID=1536179
|Title=Cystic fibrosis mutations in French Canadians: three CFTR mutations are relatively frequent in a Quebec population with an elevated incidence of cystic fibrosis.
}}

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

{{PMID Auto
|PMID=15371902
|Title=Cystic fibrosis population carrier screening: 2004 revision of American College of Medical Genetics mutation panel.
|OA=1
}}

{{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.
}}