List of variants reported as likely pathogenic for X-linked complex neurodevelopmental disorder by Mendelics

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Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_001184880.2(PCDH19):c.1442A>G (p.Asp481Gly)	rs1602636096
NM_001184880.2(PCDH19):c.1787A>G (p.Asp596Gly)	rs2147537831
NM_001184880.2(PCDH19):c.1925T>G (p.Val642Gly)	rs1602635282
NM_001184880.2(PCDH19):c.1938C>A (p.Asp646Glu)	rs1602635261
NM_001184880.2(PCDH19):c.260_292del (p.Ile87_Pro97del)	rs1602638228
NM_001184880.2(PCDH19):c.959A>T (p.Asp320Val)	rs1602636925

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