List of variants in gene NOTCH1 reported as benign by Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_017617.5(NOTCH1):c.1669+9T>C	rs3125006	0.87879
NM_017617.5(NOTCH1):c.6555C>T (p.Asp2185=)	rs2229974	0.59546
NM_017617.5(NOTCH1):c.1441+7C>T	rs9411208	0.57467
NM_017617.5(NOTCH1):c.2588-4G>A	rs3125001	0.48952
NM_017617.5(NOTCH1):c.1670-9A>G	rs3124603	0.47256
NM_017617.5(NOTCH1):c.852G>A (p.Pro284=)	rs2229975	0.12249
NM_017617.5(NOTCH1):c.3836G>A (p.Arg1279His)	rs61751543	0.01655

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