List of variants reported as likely pathogenic for bone disorder by Department of Pediatrics, National Cheng-Kung University Hospital

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001286577.2(C2CD3):c.1730G>A (p.Arg577His)	rs755686768
NM_001286577.2(C2CD3):c.2720A>G (p.Tyr907Cys)	rs2496439292
NM_003611.3(OFD1):c.1972A>T (p.Lys658Ter)	rs2518939102

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