List of variants in gene ASXL3 reported as likely benign by Center for Pediatric Genomic Medicine, Children's Mercy Hospital and Clinics

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_030632.3(ASXL3):c.1409A>C (p.His470Pro)	rs80040227	0.01034
NM_030632.3(ASXL3):c.3389C>G (p.Pro1130Arg)	rs185753602	0.00127
NM_030632.3(ASXL3):c.3350G>A (p.Arg1117Gln)	rs200723688	0.00007

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