List of variants in gene FLNA reported as benign for History of neurodevelopmental disorder

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: 24

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HGVS	dbSNP	gnomAD frequency
NM_001110556.2(FLNA):c.5850T>C (p.Ala1950=)	rs2070825	0.22980
NM_001110556.2(FLNA):c.4920G>A (p.Gly1640=)	rs61741041	0.08115
NM_001110556.2(FLNA):c.6642G>C (p.Val2214=)	rs1064822	0.05512
NM_001110556.2(FLNA):c.3035C>T (p.Ser1012Leu)	rs17091204	0.04081
NM_001110556.2(FLNA):c.5290G>A (p.Ala1764Thr)	rs57108893	0.04049
NM_001110556.2(FLNA):c.7224C>T (p.Gly2408=)	rs12008807	0.02548
NM_001110556.2(FLNA):c.1968C>T (p.Leu656=)	rs73638274	0.02319
NM_001110556.2(FLNA):c.3270C>T (p.Ile1090=)	rs79391751	0.02044
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.3690C>T (p.Thr1230=)	rs35015603	0.00732
NM_001110556.2(FLNA):c.5814C>T (p.Tyr1938=)	rs140084263	0.00624
NM_001110556.2(FLNA):c.663C>T (p.Pro221=)	rs2073470	0.00452
NM_001110556.2(FLNA):c.882A>G (p.Thr294=)	rs184864998	0.00373
NM_001110556.2(FLNA):c.1998G>A (p.Ala666=)	rs34510365	0.00316
NM_001110556.2(FLNA):c.1582G>A (p.Val528Met)	rs143873938	0.00313
NM_001110556.2(FLNA):c.4233G>A (p.Ser1411=)	rs34439033	0.00295
NM_001110556.2(FLNA):c.5972C>T (p.Ser1991Leu)	rs187029309	0.00227
NM_001110556.2(FLNA):c.7222G>A (p.Gly2408Ser)	rs201168500	0.00135
NM_001110556.2(FLNA):c.4451A>G (p.Gln1484Arg)	rs200130356	0.00081
NM_001110556.2(FLNA):c.3597G>A (p.Ser1199=)	rs200258756	0.00054
NM_001110556.2(FLNA):c.2845G>A (p.Val949Ile)	rs201656372	0.00018
NM_001110556.2(FLNA):c.4494C>T (p.Asp1498=)	rs183948518	0.00006
NM_001110556.2(FLNA):c.7067G>A (p.Ser2356Asn)	rs782739586	0.00005

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