List of variants reported as likely pathogenic for bone neoplasm by Genome Sciences Centre, British Columbia Cancer Agency

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_002430.3(MN1):c.772_776del (p.His258fs)	rs1568986076
NM_002430.3(MN1):c.785del (p.Gly262fs)	rs1568986066
NM_003482.4(KMT2D):c.11047C>T (p.Gln3683Ter)	rs1565779530

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