List of variants reported as uncertain significance for Developmental and epileptic encephalopathy, 18 by Neuberg Centre For Genomic Medicine, NCGM

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Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_001365999.1(SZT2):c.9629G>A (p.Arg3210His)	rs371193436	0.00013
NM_001365999.1(SZT2):c.4721G>A (p.Arg1574Gln)	rs532357677	0.00005
NM_001365999.1(SZT2):c.8840G>A (p.Arg2947Gln)	rs147484328	0.00004
NM_001365999.1(SZT2):c.8225G>A (p.Arg2742His)	rs763615703	0.00001
NM_001365999.1(SZT2):c.3689C>T (p.Ala1230Val)	rs553638915
NM_001365999.1(SZT2):c.6253_6255del (p.Tyr2085del)

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