List of variants reported as uncertain significance for atypical Rett syndrome by Genetic Services Laboratory, University of Chicago

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Total variants: 11

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HGVS	dbSNP	gnomAD frequency
NM_005249.5(FOXG1):c.456G>T (p.Gly152=)	rs587783637	0.00020
NM_001323289.2(CDKL5):c.283-13A>G	rs587783404	0.00011
NM_001323289.2(CDKL5):c.2200A>G (p.Thr734Ala)	rs55803460	0.00010
NM_001110792.2(MECP2):c.260C>T (p.Pro87Leu)	rs267608440	0.00003
NM_001323289.2(CDKL5):c.1678A>G (p.Thr560Ala)	rs587783400	0.00001
NM_001323289.2(CDKL5):c.2653G>A (p.Gly885Arg)	rs398123694	0.00001
NM_001323289.2(CDKL5):c.248G>T (p.Gly83Val)	rs587783402
NM_001323289.2(CDKL5):c.969G>A (p.Leu323=)	rs587783407
NM_003159.3(CDKL5):c.2820C>A (p.Asp940Glu)	rs587783403
NM_005249.5(FOXG1):c.209_235del (p.Gln70_Pro78del)	rs587783634
NM_005249.5(FOXG1):c.672C>G (p.Gly224=)	rs587783639

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