List of variants reported as uncertain significance for filamin-related bone disorder by Genomic Research Center, Shahid Beheshti University of Medical Sciences

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001110556.2(FLNA):c.2122C>T (p.Arg708Trp)	rs782287086	0.00001
NM_001110556.2(FLNA):c.546G>C (p.Gln182His)	rs1557179648	0.00001
NM_001457.4(FLNB):c.199C>T (p.His67Tyr)	rs751371914

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