List of variants in gene WAS reported as likely benign by PreventionGenetics, part of Exact Sciences

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 14

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HGVS	dbSNP	gnomAD frequency
NM_000377.3(WAS):c.995T>C (p.Val332Ala)	rs2737799	0.00489
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.90C>T (p.His30=)	rs148800063	0.00053
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.264C>T (p.Tyr88=)	rs150520117	0.00008
NM_000377.3(WAS):c.1299G>A (p.Ala433=)	rs372649110	0.00006
NM_000377.3(WAS):c.941C>T (p.Pro314Leu)	rs782752881	0.00005
NM_000377.3(WAS):c.1218C>T (p.Ser406=)	rs370053372	0.00002
NM_000377.3(WAS):c.210G>A (p.Gly70=)	rs886038288
NM_000377.3(WAS):c.273+10_273+11dup	rs58371799
NM_000377.3(WAS):c.273+11dup	rs58371799

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