{{Rsnum
|rsid=75039782
|Chromosome=7
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=CFTR
|position=117639961
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CFTR
}}{{omim
|id=602421
|rsnum=75039782
|variant=0062
}}{{ClinVar
|rsid=75039782
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=117280015
|CHROM=7
|dbSNPBuildID=131
|SSR=0
|SAO=0
|VP=0x050068000000000402110100
|GENEINFO=CFTR:1080
|GENE_NAME=CFTR
|GENE_ID=1080
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000007.13:g.117280015C>T
|CLNSRC=CFTR2; Cystic Fibrosis Mutation Database; GTR; OMIM Allelic Variant
|CLNSRCID=3849+10kbC->T; 518; GTR000257096; GTR000500233; 602421.0062
|CLNSIG=5
|CLNCUI=C0010674
|CLNDBN=Cystic fibrosis; not provided
|Disease=Cystic fibrosis; not provided
|CLNACC=RCV000007586.6; RCV000079001.1
|Tags=PM;PMC;HD;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1250:C0010674:219700:586:190905008
}}{{PMID Auto
|PMID=15948195
|Title=Mutation spectrum in Jewish cystic fibrosis patients in Israel: implication to carrier screening.
}}