List of variants in gene ASH1L reported as benign by CeGaT Center for Human Genetics Tuebingen

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_018489.3(ASH1L):c.3319A>G (p.Ile1107Val)	rs140137038	0.00126
NM_018489.3(ASH1L):c.891A>G (p.Val297=)	rs200853973	0.00004
NM_018489.3(ASH1L):c.1279G>A (p.Glu427Lys)
NM_018489.3(ASH1L):c.2940A>G (p.Lys980=)
NM_018489.3(ASH1L):c.5310C>A (p.Val1770=)	rs61732805

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