List of variants reported as uncertain significance for Infantile epilepsy syndrome

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_001032221.6(STXBP1):c.1288G>A (p.Ala430Thr)	rs148131665	0.00001
NM_001032221.6(STXBP1):c.1654T>C (p.Cys552Arg)	rs1842046459
NM_001032221.6(STXBP1):c.755T>C (p.Met252Thr)	rs1841289209
NM_003966.3(SEMA5A):c.85C>T (p.Gln29Ter)	rs2478059181

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