List of variants in gene FLNB reported as uncertain significance for Boomerang dysplasia

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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: 13

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HGVS	dbSNP	gnomAD frequency
NM_001457.4(FLNB):c.808A>G (p.Met270Val)	rs145036794	0.00096
NM_001457.4(FLNB):c.4730C>T (p.Ala1577Val)	rs148101195	0.00043
NM_001457.4(FLNB):c.1588G>T (p.Gly530Trp)	rs773943113	0.00022
NM_001457.4(FLNB):c.5917G>A (p.Glu1973Lys)	rs368965386	0.00004
NM_001457.4(FLNB):c.3724+4G>C	rs993620203	0.00003
NM_001457.4(FLNB):c.3325G>A (p.Val1109Ile)	rs200947960	0.00002
NM_001457.4(FLNB):c.3350A>G (p.His1117Arg)	rs779765790	0.00001
NM_001457.4(FLNB):c.4826C>T (p.Thr1609Ile)	rs761698437	0.00001
NM_001457.4(FLNB):c.199C>T (p.His67Tyr)	rs751371914
NM_001457.4(FLNB):c.2996G>A (p.Arg999Gln)	rs755928543
NM_001457.4(FLNB):c.4391G>C (p.Gly1464Ala)	rs886044175
NM_001457.4(FLNB):c.4589A>G (p.Tyr1530Cys)	rs776043627
NM_001457.4(FLNB):c.6866G>A (p.Arg2289His)	rs1033252725

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