List of variants reported as uncertain significance for Epilepsy by Clinical Molecular Genetics Laboratory, Johns Hopkins All Children's Hospital

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_001365536.1(SCN9A):c.328T>C (p.Ser110Pro)	rs201503351	0.00009
NM_000079.4(CHRNA1):c.410C>T (p.Thr137Met)	rs780391418	0.00003
NM_000079.4(CHRNA1):c.710A>T (p.Asn237Ile)	rs1558911753
NM_001353921.2(ARHGEF9):c.211-5C>T	rs1569481993

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