{{Rsnum
|rsid=76713772
|Gene=CFTR
|Chromosome=7
|position=117587738
|Orientation=plus
|GMAF=0.0004591
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=CFTR
}}{{omim
|id=602421
|rsnum=76713772
|variant=0008
}}{{ClinVar
|rsid=76713772
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=117227792
|CHROM=7
|GMAF=0.0005
|dbSNPBuildID=131
|SSR=0
|SAO=0
|VP=0x050068000000040416110100
|GENEINFO=CFTR:1080
|GENE_NAME=CFTR
|GENE_ID=1080
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000007.13:g.117227792G>A
|CLNSRC=CFTR2; Cystic Fibrosis Mutation Database; GTR; OMIM Allelic Variant
|CLNSRCID=1717-1G->A; 255; GTR000074114; GTR000257096; GTR000500233; 602421.0008
|CLNSIG=5
|CLNCUI=C0010674
|CLNDBN=Cystic fibrosis
|Disease=Cystic fibrosis
|CLNACC=RCV000007532.6
|Tags=PM;PMC;VLD;HD;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9995; 0.0004591
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1250:C0010674:219700:586:190905008
|COMMON=0
}}{{PMID|15948195}} Mutation spectrum in Jewish cystic fibrosis patients in Israel: implication to carrier screening.