List of variants reported as pathogenic for syndromic craniosynostosis by Institute of Human Genetics, Clinical Exome/Genome Diagnostics Group, University Hospital Bonn

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Total variants: 1

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HGVS	dbSNP	gnomAD frequency
NM_021224.6(ZNF462):c.2029del (p.Arg677fs)	rs2131465180

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