{{Rsnum
|rsid=11971167
|Gene=CFTR
|Chromosome=7
|position=117642528
|Orientation=plus
|ReferenceAllele=G
|MissenseAllele=A
|GMAF=0.003673
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=CFTR
}}[[Cystic Fibrosis]] mutation

{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 0.0 | 0.0 | 100.0
| HCB | 0.0 | 0.0 | 100.0
| JPT | 0.0 | 0.0 | 100.0
| YRI | 0.0 | 2.7 | 97.3
| ASW | 0.0 | 3.5 | 96.5
| CHB | 0.0 | 0.0 | 100.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 1.9 | 98.1
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 1.0 | 99.0
| HapMapRevision=28
}}
{{omim
|desc=VAS DEFERENS, CONGENITAL BILATERAL ABSENCE OF
|id=602421
|rsnum=11971167
|variant=0060
}}

{{ClinVar
|rsid=11971167
|Reversed=0
|FwdREF=G
|FwdALT=A,T
|REF=G
|ALT=A,T
|RSPOS=117282582
|CHROM=7
|GMAF=0.0037
|dbSNPBuildID=120
|SSR=0
|SAO=1
|VP=0x050268000000040517110100
|GENEINFO=CFTR:1080
|GENE_NAME=CFTR
|GENE_ID=1080
|WGT=0
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000007.13:g.117282582G>A; NC_000007.13:g.117282582G>T
|CLNSRC=GTR; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=GTR000257096; 602421.0060
|CLNSIG=5
|CLNCUI=CN069039
|CLNDBN=Congenital bilateral absence of the vas deferens; Cystic fibrosis
|Disease=Congenital bilateral absence of the vas deferens; Cystic fibrosis
|CLNACC=RCV000007584.1; RCV000046985.2; RCV000046986.2
|Tags=PM;PMC;S3D;VLD;HD;GNO;KGPhase1;KGPROD;OTHERKG;PH3;LSD;OM
|CAF=0.9963; 0.003673; .
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet; GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1250:CN032726:277180:48; NBK1250:C0010674:219700:586:190905008
|COMMON=1
}}

{{PMID Auto
|PMID=18716917
|Title=A novel computational and structural analysis of nsSNPs in CFTR gene.
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | Illumina Human 1M}}