List of variants reported as uncertain significance for atelosteogenesis by Centre for Mendelian Genomics, University Medical Centre Ljubljana

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_001457.4(FLNB):c.572C>T (p.Pro191Leu)	rs368472521	0.00005
NM_001457.4(FLNB):c.6164G>A (p.Gly2055Asp)	rs375752014	0.00004
NM_001457.4(FLNB):c.776C>T (p.Ala259Val)	rs376619286	0.00003
NM_001457.4(FLNB):c.2417C>A (p.Thr806Lys)	rs940585956
NM_001457.4(FLNB):c.7760G>T (p.Trp2587Leu)	rs144321868

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