List of variants reported as uncertain significance for epilepsy by Institute of Medical Genetics and Applied Genomics, University Hospital Tübingen

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_001127222.2(CACNA1A):c.781del (p.Thr261fs)	rs2059189334
NM_001134407.3(GRIN2A):c.3087T>A (p.Asn1029Lys)
NM_001165963.4(SCN1A):c.3650A>G (p.His1217Arg)	rs796052996
NM_001330260.2(SCN8A):c.2621C>T (p.Ala874Val)
NM_052874.5(STX1B):c.682A>G (p.Met228Val)

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