List of variants in gene ASXL2 reported as 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_018263.6(ASXL2):c.3674G>C (p.Cys1225Ser)	rs144145474	0.00532
NM_018263.6(ASXL2):c.1489G>A (p.Ala497Thr)	rs192716734	0.00412
NM_018263.6(ASXL2):c.3102G>T (p.Arg1034Ser)	rs144699852	0.00186

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