List of variants in gene ASXL1 reported as likely pathogenic by University of Washington Center for Mendelian Genomics, University of Washington

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_015338.6(ASXL1):c.1045C>T (p.Gln349Ter)	rs2011568558
NM_015338.6(ASXL1):c.3856C>T (p.Gln1286Ter)	rs2011901554
NM_015338.6(ASXL1):c.4243C>T (p.Arg1415Ter)	rs754129466

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