List of variants reported as likely pathogenic for electroclinical syndrome by Institute of Human Genetics, Clinical Exome/Genome Diagnostics Group, University Hospital Bonn

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001127644.2(GABRA1):c.785_786dup (p.Met263Ter)
NM_001271.4(CHD2):c.2636C>T (p.Ala879Val)	rs1555442813
NM_001330260.2(SCN8A):c.4784T>C (p.Leu1595Pro)

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