List of variants reported as uncertain significance for electroclinical syndrome by Diagnostics Services (NGS), CSIR - Centre For Cellular And Molecular Biology

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_172107.4(KCNQ2):c.1291G>A (p.Gly431Arg)	rs746853951	0.00001
NM_004519.4(KCNQ3):c.1415T>A (p.Phe472Tyr)
NM_139058.3(ARX):c.433G>T (p.Ala145Ser)	rs1438576250

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