List of variants reported as likely pathogenic for X-linked severe congenital neutropenia; Thrombocytopenia 1; Wiskott-Aldrich syndrome by Labcorp Genetics (formerly Invitae), Labcorp

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Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_000377.3(WAS):c.1339-2A>G	rs2147267240
NM_000377.3(WAS):c.142A>C (p.Thr48Pro)	rs2062412197
NM_000377.3(WAS):c.250T>C (p.Phe84Leu)	rs2147262951
NM_000377.3(WAS):c.373G>C (p.Gly125Arg)	rs2147263882
NM_000377.3(WAS):c.383T>G (p.Phe128Cys)
NM_000377.3(WAS):c.463+1G>A
NM_000377.3(WAS):c.70T>C (p.Ser24Pro)	rs2062410722

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