List of variants in gene FLCN reported as uncertain significance 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: 7

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HGVS	dbSNP	gnomAD frequency
NM_144997.7(FLCN):c.268G>T (p.Ala90Ser)	rs141140415	0.00029
NM_144997.7(FLCN):c.43G>A (p.Gly15Ser)	rs539468848	0.00004
NM_144997.7(FLCN):c.1174C>T (p.Arg392Trp)	rs1060502374	0.00002
NM_144997.7(FLCN):c.1697T>C (p.Met566Thr)	rs756302545
NM_144997.7(FLCN):c.594_596del (p.Asp198del)	rs1567819459
NM_144997.7(FLCN):c.665T>G (p.Met222Arg)	rs1555609889
NM_144997.7(FLCN):c.871+22C>T

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