List of variants in gene FLNB reported as likely benign for Connective tissue disorder

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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: 15

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HGVS	dbSNP	gnomAD frequency
NM_001457.4(FLNB):c.1919C>T (p.Thr640Met)	rs62621999	0.00943
NM_001457.4(FLNB):c.3771G>A (p.Pro1257=)	rs146851485	0.00794
NM_001457.4(FLNB):c.2907G>A (p.Arg969=)	rs138449267	0.00724
NM_001457.4(FLNB):c.3240G>A (p.Pro1080=)	rs77989135	0.00333
NM_001457.4(FLNB):c.6231C>T (p.Asp2077=)	rs145280904	0.00184
NM_001457.4(FLNB):c.4929C>T (p.Ala1643=)	rs149070858	0.00140
NM_001457.4(FLNB):c.6173A>G (p.Lys2058Arg)	rs141698427	0.00048
NM_001457.4(FLNB):c.1203C>T (p.Thr401=)	rs148507053	0.00021
NM_001457.4(FLNB):c.5785G>A (p.Asp1929Asn)	rs146685642	0.00017
NM_001457.4(FLNB):c.2931G>A (p.Leu977=)	rs574484752	0.00012
NM_001457.4(FLNB):c.1278C>T (p.His426=)	rs572259451	0.00003
NM_001457.4(FLNB):c.1107C>T (p.Asn369=)	rs538953239	0.00002
NM_001457.4(FLNB):c.5533G>A (p.Val1845Ile)	rs575434109	0.00001
NM_001457.4(FLNB):c.6755A>T (p.Tyr2252Phe)	rs200567066	0.00001
NM_001457.4(FLNB):c.107G>A (p.Arg36His)	rs142568031

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