List of variants reported as likely pathogenic for bone disorder by Institute for Genomic Statistics and Bioinformatics, University Hospital Bonn

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_022552.5(DNMT3A):c.2186G>A (p.Arg729Gln)	rs757211277	0.00001
NM_001382391.1(CSPP1):c.2381_2382del (p.Lys794fs)	rs1827118960
NM_181336.4(LEMD2):c.1436C>T (p.Ser479Phe)	rs1767330976

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