List of variants reported as pathogenic for X-linked severe congenital neutropenia; Thrombocytopenia 1; Wiskott-Aldrich syndrome by Fulgent Genetics, Fulgent Genetics

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Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_000377.3(WAS):c.223G>A (p.Val75Met)	rs782290433	0.00001
NM_000377.3(WAS):c.1090C>T (p.Arg364Ter)	rs2062429013
NM_000377.3(WAS):c.134C>T (p.Thr45Met)	rs132630273
NM_000377.3(WAS):c.1453G>A (p.Asp485Asn)	rs1064793293
NM_000377.3(WAS):c.238C>T (p.Gln80Ter)	rs2062412730
NM_000377.3(WAS):c.256C>T (p.Arg86Cys)	rs2062412810
NM_000377.3(WAS):c.37C>T (p.Arg13Ter)	rs193922415
NM_000377.3(WAS):c.691A>T (p.Lys231Ter)
NM_000377.3(WAS):c.913C>T (p.Gln305Ter)

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