{{Rsnum
|rsid=80338683
|Chromosome=17
|Orientation=minus
|geno1=(-;-)
|geno2=(-;C)
|geno3=(C;C)
|Gene=FLCN
|position=17216395
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=FLCN,LOC101928660
}}{{omim
|id=607273
|rsnum=80338683
|variant=0002
}}{{ClinVar
|rsid=80338683
|Reversed=1
|FwdREF=C
|FwdALT=
|REF=TG
|ALT=T
|RSPOS=17119708
|CHROM=17
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050168000000000002110200
|GENEINFO=FLCN:201163
|GENE_NAME=FLCN
|GENE_ID=201163
|WGT=0
|VC=DIV
|CLNALLE=1
|CLNHGVS=NC_000017.10:g.17119709delG
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=NBK1522; 607273.0002
|CLNSIG=5
|CLNCUI=C0346010; C0346010
|CLNDBN=Multiple fibrofolliculomas; not provided
|Disease=Multiple fibrofolliculomas; not provided
|CLNACC=RCV000003531.1; RCV000082625.1
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1522:C0346010:135150:122:110985001
}}{{PMID|12204536}} 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|15852235|OA=1
}} Germline BHD-mutation spectrum and phenotype analysis of a large cohort of families with Birt-Hogg-Dube syndrome.