List of variants reported as uncertain significance for bone development disease by Undiagnosed Diseases Network, NIH

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Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_000088.4(COL1A1):c.104-284C>T	rs2144595908
NM_004208.4(AIFM1):c.760G>A (p.Glu254Lys)	rs2124656997
NM_015909.4(NBAS):c.2423+403G>C
NM_018060.4(IARS2):c.1562G>A (p.Cys521Tyr)
NM_018060.4(IARS2):c.2186C>T (p.Thr729Ile)
NR_023343.3(RNU4ATAC):n.47T>G	rs767236617

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