{{Rsnum
|rsid=121908761
|Chromosome=7
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=CFTR
|position=117611717
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CFTR
}}{{omim
|id=602421
|rsnum=121908761
|variant=0106
}}{{ClinVar
|rsid=121908761
|Reversed=0
|FwdREF=C
|FwdALT=A,G
|REF=C
|ALT=A,G
|RSPOS=117251771
|CHROM=7
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050068000000000002110100
|GENEINFO=CFTR:1080
|GENE_NAME=CFTR
|GENE_ID=1080
|WGT=0
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000007.13:g.117251771C>A; NC_000007.13:g.117251771C>G
|CLNORIGIN=1
|CLNSRCID=
Y1092X_47333; GTR000257096; GTR000500233; Y1092X_22250; GTR000074114; 602421.0106
|CLNSIG=5
|CLNCUI=
|CLNACC=
RCV000007632.1; RCV000056379.2; RCV000056380.2
|Tags=PM;PMC;OTHERKG;LSD;OM
|CLNDBN=Cystic fibrosis
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1250:C0010674:219700:586:190905008
|CLNSRC=CFTR2; GTR; OMIM Allelic Variant
|Disease=Cystic fibrosis
}}{{PMID Auto
|PMID=2671335
|Title=Pneumatosis intestinalis in children beyond the neonatal period.
}}

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