List of variants reported as uncertain significance for Cardiac valvular dysplasia, X-linked; FG syndrome 2; Heterotopia, periventricular, X-linked dominant; Intestinal pseudoobstruction, neuronal, chronic idiopathic, X-linked; Melnick-Needles syndrome; Oto-palato-digital syndrome, type I; Oto-palato-digital syndrome, type II; Terminal osseous dysplasia-pigmentary defects syndrome; Frontometaphyseal dysplasia 1

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Total variants: 37

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HGVS	dbSNP	gnomAD frequency
NM_001110556.2(FLNA):c.901C>T (p.Arg301Trp)	rs192609440	0.00007
NM_001110556.2(FLNA):c.5138C>T (p.Thr1713Met)	rs782555986	0.00004
NM_001110556.2(FLNA):c.1019G>A (p.Arg340His)	rs371368679	0.00003
NM_001110556.2(FLNA):c.4517C>T (p.Thr1506Ile)	rs797045579	0.00003
NM_001110556.2(FLNA):c.4625C>T (p.Thr1542Ile)	rs782281134	0.00003
NM_001110556.2(FLNA):c.6863G>A (p.Arg2288His)	rs782275601	0.00003
NM_001110556.2(FLNA):c.1060C>T (p.His354Tyr)	rs1489530369	0.00002
NM_001110556.2(FLNA):c.1633A>G (p.Met545Val)	rs1443563081	0.00002
NM_001110556.2(FLNA):c.2392G>A (p.Glu798Lys)	rs782454177	0.00002
NM_001110556.2(FLNA):c.2974A>G (p.Thr992Ala)	rs782445995	0.00002
NM_001110556.2(FLNA):c.6376C>T (p.Pro2126Ser)	rs782400832	0.00002
NM_001110556.2(FLNA):c.1270A>G (p.Met424Val)	rs782066542	0.00001
NM_001110556.2(FLNA):c.1823C>T (p.Thr608Met)	rs1603362434	0.00001
NM_001110556.2(FLNA):c.2254G>A (p.Val752Ile)	rs1297013254	0.00001
NM_001110556.2(FLNA):c.2410G>A (p.Val804Ile)	rs374130804	0.00001
NM_001110556.2(FLNA):c.2590G>T (p.Val864Phe)	rs1557178198	0.00001
NM_001110556.2(FLNA):c.2981A>G (p.Lys994Arg)	rs3819330	0.00001
NM_001110556.2(FLNA):c.3323G>A (p.Cys1108Tyr)	rs371677498	0.00001
NM_001110556.2(FLNA):c.4474+3G>T	rs1286863443	0.00001
NM_001110556.2(FLNA):c.569G>A (p.Arg190Gln)	rs782447567	0.00001
NM_001110556.2(FLNA):c.6719A>G (p.Lys2240Arg)	rs797045581	0.00001
NM_001110556.2(FLNA):c.6725G>A (p.Arg2242Gln)	rs781984274	0.00001
NM_001110556.2(FLNA):c.1204A>G (p.Thr402Ala)	rs1569551838
NM_001110556.2(FLNA):c.1396C>T (p.Pro466Ser)
NM_001110556.2(FLNA):c.2464A>G (p.Ile822Val)	rs2148114467
NM_001110556.2(FLNA):c.2792A>T (p.Asn931Ile)	rs1557178134
NM_001110556.2(FLNA):c.289C>T (p.Pro97Ser)
NM_001110556.2(FLNA):c.3034T>G (p.Ser1012Ala)	rs1364359427
NM_001110556.2(FLNA):c.3122A>G (p.Tyr1041Cys)
NM_001110556.2(FLNA):c.3670C>T (p.Leu1224Phe)	rs1557177690
NM_001110556.2(FLNA):c.4314C>G (p.Phe1438Leu)	rs1557177412
NM_001110556.2(FLNA):c.4730A>G (p.Glu1577Gly)	rs2148110326
NM_001110556.2(FLNA):c.494A>G (p.Lys165Arg)	rs1569551874
NM_001110556.2(FLNA):c.5406C>T (p.Gly1802=)
NM_001110556.2(FLNA):c.568C>T (p.Arg190Trp)
NM_001110556.2(FLNA):c.674C>T (p.Ala225Val)
NM_001110556.2(FLNA):c.7628G>A (p.Cys2543Tyr)

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