{{Rsnum
|rsid=121909005
|Chromosome=7
|Orientation=plus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=CFTR
|position=117587801
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CFTR
}}{{omim
|id=602421
|rsnum=121909005
|variant=0012
}}{{ClinVar
|rsid=121909005
|Reversed=0
|FwdREF=T
|FwdALT=G
|REF=T
|ALT=G
|RSPOS=117227855
|CHROM=7
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=CFTR:1080
|GENE_NAME=CFTR
|GENE_ID=1080
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000007.13:g.117227855T>G
|CLNSRC=CFTR2; GTR; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=S549R_22157; GTR000074114; GTR000257096; 602421.0012
|CLNSIG=5
|CLNCUI=C0010674; C0010674; C0010674
|CLNDBN=Cystic fibrosis
|Disease=Cystic fibrosis
|CLNACC=RCV000007538.1; RCV000056350.2
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1250:C0010674:219700:586:190905008
}}