List of variants reported as likely pathogenic for electroclinical syndrome by Blueprint Genetics

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001271.4(CHD2):c.1126C>T (p.Gln376Ter)	rs2053431254
NM_001271.4(CHD2):c.2190-1G>C	rs2053845402
NM_001323289.2(CDKL5):c.473G>C (p.Arg158Pro)	rs757402424

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