List of variants in gene FLNA reported as likely benign by Fulgent Genetics, Fulgent Genetics

Minimum submission review status:		Collection method:
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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 14

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HGVS	dbSNP	gnomAD frequency
NM_001110556.2(FLNA):c.3035C>T (p.Ser1012Leu)	rs17091204	0.04081
NM_001110556.2(FLNA):c.3690C>T (p.Thr1230=)	rs35015603	0.00732
NM_001110556.2(FLNA):c.1176G>A (p.Glu392=)	rs201173693	0.00446
NM_001110556.2(FLNA):c.5972C>T (p.Ser1991Leu)	rs187029309	0.00227
NM_001110556.2(FLNA):c.7267C>T (p.Pro2423Ser)	rs200198847	0.00046
NM_001110556.2(FLNA):c.3207+14G>A	rs200710010	0.00041
NM_001110556.2(FLNA):c.3421G>A (p.Ala1141Thr)	rs201908251	0.00025
NM_001110556.2(FLNA):c.2516C>T (p.Thr839Met)	rs201603843	0.00022
NM_001110556.2(FLNA):c.4908C>T (p.Ala1636=)	rs367979917	0.00009
NM_001110556.2(FLNA):c.1581C>T (p.Arg527=)	rs782684339	0.00008
NM_001110556.2(FLNA):c.5283C>T (p.Tyr1761=)	rs782313331	0.00002
NM_001110556.2(FLNA):c.2316C>A (p.Val772=)	rs2067723075	0.00001
NM_001110556.2(FLNA):c.3387C>T (p.Thr1129=)	rs372874251
NM_001110556.2(FLNA):c.7326T>C (p.Gly2442=)	rs1026564714

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