List of variants in gene ASXL1 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_015338.6(ASXL1):c.3503G>C (p.Ser1168Thr)	rs587778062	0.00010
NM_015338.6(ASXL1):c.2618C>T (p.Pro873Leu)	rs202098158	0.00006
NM_015338.6(ASXL1):c.314C>T (p.Thr105Met)	rs749495615	0.00001

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