List of variants in gene FLCN reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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: 13

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HGVS	dbSNP	gnomAD frequency
NM_144997.7(FLCN):c.1333G>A (p.Ala445Thr)	rs41419545	0.00217
NM_144997.7(FLCN):c.959G>A (p.Arg320Gln)	rs143483053	0.00071
NM_144997.7(FLCN):c.*695C>T	rs775700421	0.00058
NM_144997.7(FLCN):c.871+47G>A	rs142934950	0.00058
NM_144997.7(FLCN):c.1269C>T (p.His423=)	rs41464156	0.00053
NM_144997.7(FLCN):c.1149C>T (p.Leu383=)	rs150752548	0.00028
NM_144997.7(FLCN):c.246C>T (p.Cys82=)	rs150712346	0.00020
NM_144997.7(FLCN):c.1278C>T (p.Ile426=)	rs41459448	0.00016
NM_144997.7(FLCN):c.1281C>G (p.Pro427=)	rs372207262	0.00014
NM_144997.7(FLCN):c.687C>T (p.Phe229=)	rs754710935	0.00008
NM_144997.7(FLCN):c.429C>T (p.Phe143=)	rs773792624	0.00003
NM_144997.7(FLCN):c.207C>T (p.Val69=)	rs759772780	0.00001
NM_144997.7(FLCN):c.42C>T (p.His14=)	rs766288960	0.00001

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