List of variants in gene combination LOC126860794, NOTCH1 reported as likely benign by CHEO Genetics Diagnostic Laboratory, Children's Hospital of Eastern Ontario

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_017617.5(NOTCH1):c.6082+10C>T	rs114120958	0.00019
NM_017617.5(NOTCH1):c.5995C>T (p.Leu1999=)	rs1208814818	0.00001
NM_017617.5(NOTCH1):c.6057C>G (p.Ala2019=)	rs758702512

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