List of variants studied for epilepsy by Department of Clinical Genetics, Medical University of Lodz

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		ClinVar version:

Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_001165963.4(SCN1A):c.4880A>T (p.Lys1627Met)
NM_001165963.4(SCN1A):c.671T>C (p.Leu224Ser)	rs796053091
NM_001199107.2(TBC1D24):c.32A>G (p.Asp11Gly)
NM_001330260.2(SCN8A):c.2507A>T (p.Asp836Val)
NM_006772.3(SYNGAP1):c.2793_2794del (p.Phe932fs)	rs1554122252
NM_006772.3(SYNGAP1):c.427C>T (p.Arg143Ter)	rs397514741
NM_006922.4(SCN3A):c.694+2T>G
NM_172107.4(KCNQ2):c.641G>A (p.Arg214Gln)	rs1057518555

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