List of variants reported as uncertain significance for electroclinical syndrome by RettBASE

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_001323289.2(CDKL5):c.904C>T (p.Leu302Phe)	rs267608547	0.00001
NM_001323289.2(CDKL5):c.1400A>C (p.His467Pro)	rs267608631
NM_001323289.2(CDKL5):c.679_691delinsGATCGTGGAA (p.Leu227_Pro231delinsAspArgGlyThr)	rs869312851
NM_001323289.2(CDKL5):c.872G>A (p.Cys291Tyr)	rs267606714

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