List of variants reported as likely pathogenic for electroclinical syndrome by Centre for Mendelian Genomics, University Medical Centre Ljubljana

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001040142.2(SCN2A):c.4801G>A (p.Val1601Met)	rs1553463140
NM_001130438.3(SPTAN1):c.6917GCATGC[3] (p.Arg2308_Met2309dup)	rs796053335
NM_004519.4(KCNQ3):c.688C>T (p.Arg230Cys)	rs796052676

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