"Center for Pediatric Genomic Medicine, Children's Mercy Hospital and - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 377157	NM_018263.6(ASXL2):c.4111C>A (p.Gln1371Lys)	ASXL2 (Q1371K +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign/Likely benign
Select item 445713	NM_018263.6(ASXL2):c.140+186A>G	ASXL2	Single nucleotide variant (intron variant)	not provided	GBenign/Likely benign