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

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Total variants: 16

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HGVS	dbSNP	gnomAD frequency
NM_000377.3(WAS):c.391G>A (p.Glu131Lys)	rs146220228	0.00222
NM_000377.3(WAS):c.1453+16C>T	rs200543049	0.00115
NM_000377.3(WAS):c.873C>T (p.Tyr291=)	rs149123892	0.00029
NM_000377.3(WAS):c.1110A>C (p.Pro370=)	rs782244198	0.00028
NM_000377.3(WAS):c.1339-18G>A	rs370010448	0.00020
NM_000377.3(WAS):c.1191G>A (p.Pro397=)	rs782486251	0.00019
NM_000377.3(WAS):c.1280C>T (p.Pro427Leu)	rs782307200	0.00019
NM_000377.3(WAS):c.559+3G>A	rs782645822	0.00010
NM_000377.3(WAS):c.273+14C>T	rs782249573	0.00006
NM_000377.3(WAS):c.339C>T (p.Phe113=)	rs782233413	0.00003
NM_000377.3(WAS):c.420C>T (p.Leu140=)	rs782639067	0.00002
NM_000377.3(WAS):c.867T>C (p.Leu289=)	rs781855402	0.00001
NM_000377.3(WAS):c.897G>A (p.Gly299=)	rs782793103	0.00001
NM_000377.3(WAS):c.470G>A (p.Arg157His)	rs369850591
NM_000377.3(WAS):c.498C>G (p.Ala166=)	rs2147264155
NM_000377.3(WAS):c.560-5dup	rs782563873

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