List of variants reported as likely pathogenic for epilepsy by Department of Clinical Genetics, Medical University of Lodz

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001165963.4(SCN1A):c.4880A>T (p.Lys1627Met)
NM_001330260.2(SCN8A):c.2507A>T (p.Asp836Val)
NM_006922.4(SCN3A):c.694+2T>G

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