List of variants in gene FLCN reported as not provided for Birt-Hogg-Dube syndrome

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: 8

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HGVS	dbSNP	gnomAD frequency
NM_144997.7(FLCN):c.1085G>A (p.Arg362His)	rs559055296
NM_144997.7(FLCN):c.1285del (p.His429fs)	rs80338682
NM_144997.7(FLCN):c.1285dup (p.His429fs)	rs80338682
NM_144997.7(FLCN):c.1389C>G (p.Tyr463Ter)	rs137852929
NM_144997.7(FLCN):c.1420G>A (p.Ala474Thr)	rs2046876810
NM_144997.7(FLCN):c.296del (p.Asp99fs)	rs398124534
NM_144997.7(FLCN):c.584del (p.Gly195fs)	rs878855217
NM_144997.7(FLCN):c.610_611delinsTA (p.Ala204Ter)	rs398124538

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