List of variants reported as uncertain significance for atypical Rett syndrome by Fulgent Genetics, Fulgent Genetics

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Total variants: 11

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HGVS	dbSNP	gnomAD frequency
NM_001110792.2(MECP2):c.1469G>A (p.Arg490Gln)	rs145790362	0.00005
NM_001323289.2(CDKL5):c.2243A>G (p.Asn748Ser)	rs748459878	0.00005
NM_001110792.2(MECP2):c.838C>T (p.Arg280Trp)	rs61750239	0.00004
NM_001110792.2(MECP2):c.1291C>T (p.Pro431Ser)	rs140258520	0.00003
NM_001110792.2(MECP2):c.1049C>G (p.Thr350Ser)	rs786204313	0.00002
NM_001110792.2(MECP2):c.553C>G (p.Pro185Ala)	rs61748427	0.00002
NM_000330.4(RS1):c.326+1159C>G	rs587783160	0.00001
NM_001323289.2(CDKL5):c.1196A>C (p.Asn399Thr)	rs267608611	0.00001
NM_005249.5(FOXG1):c.194_214del (p.Pro65_Gln71del)
NM_005249.5(FOXG1):c.28G>A (p.Val10Met)
NM_005249.5(FOXG1):c.436_438del (p.Glu146del)	rs751048593

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