List of variants in gene FLCN reported as likely pathogenic for carcinoma

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.779+1G>T	rs758175953	0.00001
NM_144997.7(FLCN):c.1357_1363del (p.Gly453fs)	rs1131690841
NM_144997.7(FLCN):c.1657T>C (p.Trp553Arg)	rs1131690833
NM_144997.7(FLCN):c.189del (p.Ala64fs)	rs876660611

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