List of variants in gene ASH1L reported as likely benign by Department of Genetics, Rouen University Hospital, Normandy Center for Genomic and Personalized Medicine

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.7622C>T (p.Ala2541Val)	rs1017867504	0.00001
NM_018489.3(ASH1L):c.4400C>G (p.Pro1467Arg)	rs1665727859
NM_018489.3(ASH1L):c.6218G>A (p.Arg2073His)	rs376223781
NM_018489.3(ASH1L):c.731C>T (p.Thr244Ile)	rs2527207480
NM_018489.3(ASH1L):c.8771T>C (p.Leu2924Pro)	rs1652468987

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