List of variants in gene FLCN reported as likely pathogenic for female reproductive organ cancer

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_144997.7(FLCN):c.502C>T (p.Arg168Cys)	rs587778367	0.00001
NM_144997.7(FLCN):c.562T>A (p.Phe188Ile)	rs1407566775	0.00001
NM_144997.7(FLCN):c.437A>T (p.Glu146Val)
NM_144997.7(FLCN):c.538A>C (p.Ile180Leu)

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