List of variants reported as uncertain significance for electroclinical syndrome by Broad Center for Mendelian Genomics, Broad Institute of MIT and Harvard

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001134407.3(GRIN2A):c.3042G>A (p.Trp1014Ter)	rs1306036000
NM_001191061.2(SLC25A22):c.191G>T (p.Gly64Val)
NM_001271.4(CHD2):c.4173del (p.Lys1391fs)	rs749969667

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