List of variants in gene WAS reported as likely benign by Genetic Services Laboratory, University of Chicago

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_000377.3(WAS):c.1276G>T (p.Ala426Ser)	rs201085962	0.00160
NM_000377.3(WAS):c.538C>A (p.His180Asn)	rs145040665	0.00063
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.285G>A (p.Leu95=)	rs781799471	0.00008
NM_000377.3(WAS):c.1188A>C (p.Pro396=)	rs1557007268
NM_000377.3(WAS):c.470G>A (p.Arg157His)	rs369850591

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