List of variants in gene FLNA reported as benign by Genetic Services Laboratory, University of Chicago

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: 16

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HGVS	dbSNP	gnomAD frequency
NM_001110556.2(FLNA):c.1286C>T (p.Thr429Met)	rs36051194	0.01499
NM_001110556.2(FLNA):c.7434G>A (p.Glu2478=)	rs74667788	0.01349
NM_001110556.2(FLNA):c.2433C>T (p.Ala811=)	rs35986650	0.01258
NM_001110556.2(FLNA):c.4598+8G>C	rs112379782	0.01252
NM_001110556.2(FLNA):c.869-7C>T	rs143311779	0.01084
NM_001110556.2(FLNA):c.6742C>T (p.Leu2248=)	rs113510895	0.00698
NM_001110556.2(FLNA):c.5814C>T (p.Tyr1938=)	rs140084263	0.00624
NM_001110556.2(FLNA):c.1176G>A (p.Glu392=)	rs201173693	0.00446
NM_001110556.2(FLNA):c.882A>G (p.Thr294=)	rs184864998	0.00373
NM_001110556.2(FLNA):c.5972C>T (p.Ser1991Leu)	rs187029309	0.00227
NM_001110556.2(FLNA):c.1875C>T (p.Asp625=)	rs200660642	0.00140
NM_001110556.2(FLNA):c.6516G>A (p.Gln2172=)	rs199802825	0.00136
NM_001110556.2(FLNA):c.6023-10C>G	rs72616474	0.00127
NM_001110556.2(FLNA):c.4451A>G (p.Gln1484Arg)	rs200130356	0.00081
NM_001110556.2(FLNA):c.4866C>T (p.Tyr1622=)	rs200835571	0.00065
NM_001110556.2(FLNA):c.3429C>G (p.Thr1143=)	rs183899917

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