List of variants in gene ASXL3 reported as likely benign for Intellectual disability

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_030632.3(ASXL3):c.6359C>T (p.Ala2120Val)	rs151081332	0.00217
NM_030632.3(ASXL3):c.6346G>A (p.Ala2116Thr)	rs117661115	0.00208
NM_030632.3(ASXL3):c.1733C>T (p.Ser578Phe)	rs199871043	0.00008
NM_030632.3(ASXL3):c.3040-8C>T	rs1268795000

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