List of variants reported as likely pathogenic for dysostosis by Diagnostics Services (NGS), CSIR - Centre For Cellular And Molecular Biology

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_019074.4(DLL4):c.1396T>C (p.Cys466Arg)
NM_021224.6(ZNF462):c.4828C>T (p.Gln1610Ter)
NM_024646.3(ZYG11B):c.628C>T (p.Arg210Ter)	rs1365622597

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