List of variants in gene FLCN reported as likely pathogenic by Invitae

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: 22

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HGVS	dbSNP	gnomAD frequency
NM_144997.7(FLCN):c.1433-2A>G	rs398124528	0.00001
NC_000017.11:g.(?_17223916)_(17224149_?)del
NM_144997.7(FLCN):c.1063-2A>G	rs2144871276
NM_144997.7(FLCN):c.1176+1G>C	rs1555607929
NM_144997.7(FLCN):c.1176+2T>A	rs2046947920
NM_144997.7(FLCN):c.1176G>A (p.Arg392=)
NM_144997.7(FLCN):c.1300+1G>A	rs879255676
NM_144997.7(FLCN):c.1300+1G>C	rs879255676
NM_144997.7(FLCN):c.1300+2T>A
NM_144997.7(FLCN):c.1300+5G>C	rs746264578
NM_144997.7(FLCN):c.1301-2A>G	rs1555607296
NM_144997.7(FLCN):c.1301-2del
NM_144997.7(FLCN):c.1301-7_1304del	rs878854340
NM_144997.7(FLCN):c.1433-1_1433delinsTC
NM_144997.7(FLCN):c.1433-2A>C	rs398124528
NM_144997.7(FLCN):c.1539-2A>G	rs878855214
NM_144997.7(FLCN):c.249+1G>A
NM_144997.7(FLCN):c.249+1G>T	rs1060502369
NM_144997.7(FLCN):c.249+2del
NM_144997.7(FLCN):c.396+1G>A	rs2145009900
NM_144997.7(FLCN):c.871+2T>C
NM_144997.7(FLCN):c.872-1G>T	rs1567813248

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