List of variants reported as likely pathogenic for Developmental and epileptic encephalopathy, 11 by Neuberg Centre For Genomic Medicine, NCGM

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_001040142.2(SCN2A):c.2674G>A (p.Val892Ile)	rs121917751
NM_001040142.2(SCN2A):c.4494C>G (p.Tyr1498Ter)	rs2468129607
NM_001040142.2(SCN2A):c.4886G>A (p.Arg1629His)	rs796053157
NM_001040142.2(SCN2A):c.605C>T (p.Ala202Val)	rs1553567409

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