Variant: rs1060502368 

    present in Gene: FLCN
    present in Chromosome: 17
    Position on Chromosome: 17219060
    Alleles of this Variant: G/-

rs1060502368 in FLCN gene and Multiple fibrofolliculomas PMID 15852235 2005 Germline BHD-mutation spectrum and phenotype analysis of a large cohort of families with Birt-Hogg-Dubé syndrome.

rs1060502368 in FLCN gene and Neoplastic Syndromes, Hereditary PMID 15852235 2005 Germline BHD-mutation spectrum and phenotype analysis of a large cohort of families with Birt-Hogg-Dubé syndrome.