List of variants reported as likely pathogenic for syndromic intellectual disability by Center for Human Genetics, Inc, Center for Human Genetics, Inc

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Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_001184880.2(PCDH19):c.1815C>G (p.Tyr605Ter)	rs1057521256
NM_004586.3(RPS6KA3):c.1308C>A (p.Cys436Ter)	rs1160828151
NM_004586.3(RPS6KA3):c.1964del (p.Leu655fs)	rs1555924704
NM_004586.3(RPS6KA3):c.774+1G>C	rs1555939331
NM_014795.4(ZEB2):c.1168del (p.Ile390fs)	rs1553961747
NM_014795.4(ZEB2):c.247dup (p.Glu83fs)	rs1553964145
NM_014795.4(ZEB2):c.3023T>G (p.Phe1008Cys)	rs1553961332
NM_014795.4(ZEB2):c.3200C>A (p.Ser1067Ter)	rs1423851170

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