List of variants reported as pathogenic for autism, susceptiblity to by Centre for Mendelian Genomics, University Medical Centre Ljubljana

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_001110792.2(MECP2):c.1200_1243del (p.Pro400_Pro401insTer)	rs61752992
NM_001110792.2(MECP2):c.1244dup (p.Pro415_Glu416insTer)	rs781843758
NM_001110792.2(MECP2):c.352C>T (p.Arg118Trp)	rs28934907
NM_001110792.2(MECP2):c.844C>T (p.Arg282Ter)	rs61750240
NM_001170629.2(CHD8):c.4009C>T (p.Arg1337Ter)	rs397514552

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