{{Rsnum
|rsid=78655421
|Chromosome=7
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=CFTR
|position=117530975
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CFTR
}}{{omim
|id=602421
|rsnum=78655421
|variant=0005
}}{{ClinVar
|rsid=78655421
|Reversed=0
|FwdREF=G
|FwdALT=A,C,T
|REF=G
|ALT=A,C,T
|RSPOS=117171029
|CHROM=7
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050060000000040402110104
|GENEINFO=CFTR:1080
|GENE_NAME=CFTR
|GENE_ID=1080
|WGT=0
|VC=SNV
|CLNALLE=1; 2; 3
|CLNHGVS=NC_000007.13:g.117171029G>A; NC_000007.13:g.117171029G>C; NC_000007.13:g.117171029G>T
|CLNSRC=Emory University; GTR; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=206; GTR000074114; GTR000257096; GTR000500233; 602421.0005
|CLNSIG=5
|CLNCUI=C0010674; CN069039
|CLNDBN=Cystic fibrosis; Congenital bilateral absence of the vas deferens; not provided
|Disease=Cystic fibrosis; Congenital bilateral absence of the vas deferens; not provided
|CLNACC=RCV000007528.5; RCV000007529.1; RCV000078997.1; RCV000046918.2; RCV000046919.2
|Tags=PM;VLD;HD;OTHERKG;LSD;OM;NOV
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT; GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1250:C0010674:219700:586:190905008; NBK1250:CN032726:277180:48
}}