List of variants studied for filamin-related bone disorder by New York Genome Center

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_001457.4(FLNB):c.5059T>C (p.Tyr1687His)	rs774862180	0.00001
NM_001457.4(FLNB):c.1346-2A>G	rs757004353
NM_001457.4(FLNB):c.6866G>A (p.Arg2289His)	rs1033252725
NM_001457.4(FLNB):c.7351C>G (p.Leu2451Val)	rs2107340030
NM_145331.3(MAP3K7):c.795TTG[1] (p.Cys266del)	rs2127974453

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