List of variants in gene FLCN reported as benign by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_144997.7(FLCN):c.1433-38A>G	rs34235236	0.21634
NM_144997.7(FLCN):c.726A>T (p.Thr242=)	rs113938514	0.02907
NM_144997.7(FLCN):c.872-13A>G	rs114970273	0.01651
NM_144997.7(FLCN):c.1278C>T (p.Ile426=)	rs41459448	0.00016
NM_144997.7(FLCN):c.75G>A (p.Leu25=)	rs200350612

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