List of variants reported as uncertain significance for electroclinical syndrome by Foundation for Research in Genetics and Endocrinology, FRIGE's Institute of Human Genetics

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_004519.4(KCNQ3):c.1552G>A (p.Ala518Thr)	rs745463637	0.00001
NM_145239.3(PRRT2):c.839T>C (p.Met280Thr)	rs1419914220	0.00001
NM_000814.6(GABRB3):c.1280A>G (p.His427Arg)

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