{{Rsnum
|rsid=78802634
|Chromosome=7
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=CFTR
|position=117611707
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CFTR
}}{{omim
|id=602421
|rsnum=78802634
|variant=0088
}}{{ClinVar
|rsid=78802634
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=117251761
|CHROM=7
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050068000000000402110100
|GENEINFO=CFTR:1080
|GENE_NAME=CFTR
|GENE_ID=1080
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000007.13:g.117251761G>A
|CLNSRC=CFTR2; GTR; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=W1089X; GTR000074114; 602421.0088
|CLNSIG=5
|CLNCUI=C0010674
|CLNDBN=Cystic fibrosis
|Disease=Cystic fibrosis
|CLNACC=RCV000007615.5
|Tags=PM;PMC;HD;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1250:C0010674:219700:586:190905008
}}{{PMID|153719}} Electromagnetic measurements of metacarpal and digital blood flow in the pony.

{{PMID|1284534}} Mutations and sequence variations detected in the cystic fibrosis transmembrane conductance regulator (CFTR) gene: a report from the Cystic Fibrosis Genetic Analysis Consortium.

{{PMID|10794365}} Molecular analysis in Brazilian cystic fibrosis patients reveals five novel mutations.

{{PMID|10923036}} Spectrum of CFTR mutations in cystic fibrosis and in congenital absence of the vas deferens in France.

{{PMID|11336401}} Prevalence of cystic fibrosis mutations in Israeli Jews.

{{PMID|15948195}} Mutation spectrum in Jewish cystic fibrosis patients in Israel: implication to carrier screening.