{{Rsnum
|rsid=80338682
|Chromosome=17
|Orientation=minus
|geno1=(-;-)
|geno2=(-;C)
|geno3=(C;C)
|Gene=FLCN
|position=17216394
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=FLCN
}}{{omim
|id=607273
|rsnum=80338682
|variant=0001
}}{{ClinVar
|rsid=80338682
|Reversed=1
|FwdREF=CAG
|FwdALT=C
|REF=T
|ALT=TG
|RSPOS=17119708
|CHROM=17
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050168000000000002110200
|WGT=0
|VC=DIV
|CLNALLE=1
|CLNHGVS=NC_000017.10:g.17119709dupG
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=NBK1522; 607273.0001
|CLNSIG=5
|CLNCUI=C0346010; C1868193; C0346010
|CLNDBN=Multiple fibrofolliculomas; Pneumothorax, primary spontaneous; not provided
|Disease=Multiple fibrofolliculomas; Pneumothorax; not provided
|CLNACC=RCV000003529.1; RCV000003530.1; RCV000082626.1
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT; MedGen:OMIM
|CLNDSDBID=NBK1522:C0346010:135150:122:110985001; C1868193:173600
|GENEINFO=FLCN:201163
|GENE_ID=201163
|GENE_NAME=FLCN
}}{{PMID Auto
|PMID=12204536
|Title=Mutations in a novel gene lead to kidney tumors, lung wall defects, and benign tumors of the hair follicle in patients with the Birt-Hogg-Dube syndrome.
}}

{{PMID Auto
|PMID=12471204
|Title=Clinical and genetic studies of Birt-Hogg-Dube syndrome.
|OA=1
}}

{{PMID Auto
|PMID=15852235
|Title=Germline BHD-mutation spectrum and phenotype analysis of a large cohort of families with Birt-Hogg-Dube syndrome.
|OA=1
}}

{{PMID Auto
|PMID=17496196
|Title=Mutations of the Birt Hogg Dube gene in patients with multiple lung cysts and recurrent pneumothorax.
|OA=1
}}

{{PMID Auto
|PMID=18505456
|Title=Mutation analysis of the FLCN gene in Chinese patients with sporadic and familial isolated primary spontaneous pneumothorax.
}}