List of variants in gene ASXL1 reported as uncertain significance by New York Genome Center

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.2029C>T (p.Pro677Ser)	rs2145361163
NM_015338.6(ASXL1):c.3915T>G (p.Phe1305Leu)	rs2145389443
NM_015338.6(ASXL1):c.4624_4626TAA[1] (p.Ter1542_Ter(1542_?)(?))	rs2145398075

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