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

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Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_001130823.3(DNMT1):c.1645-1G>T	rs1568234664
NM_001386298.1(CIC):c.3017_3018insT (p.Gly1008fs)	rs1568503055
NM_001386298.1(CIC):c.3370C>T (p.Arg1124Trp)	rs1568504941
NM_003482.4(KMT2D):c.11047C>T (p.Gln3683Ter)	rs1565779530
inv(22)(q12.2q12.2)
t(5;22)(q31.2;q12.1)

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