List of variants in gene WAS reported as uncertain significance 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: 8

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HGVS	dbSNP	gnomAD frequency
NM_000377.3(WAS):c.1181C>T (p.Pro394Leu)	rs373524969	0.00031
NM_000377.3(WAS):c.1252G>T (p.Ala418Ser)	rs782784813	0.00005
NM_000377.3(WAS):c.1150C>T (p.Pro384Ser)	rs782761074	0.00004
NM_000377.3(WAS):c.1080A>C (p.Pro360=)	rs1409607754
NM_000377.3(WAS):c.1191G>C (p.Pro397=)	rs782486251
NM_000377.3(WAS):c.1267G>C (p.Gly423Arg)	rs782711732
NM_000377.3(WAS):c.407_408delinsTT (p.Ala136Val)	rs2147263947
NM_000377.3(WAS):c.548G>A (p.Gly183Glu)	rs2147264317

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