List of variants in gene NOTCH1 reported as uncertain significance by Genome Diagnostics Laboratory, Amsterdam University Medical Center

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.3001G>A (p.Gly1001Ser)	rs763621169	0.00006
NM_017617.5(NOTCH1):c.4492A>G (p.Lys1498Glu)	rs745681787	0.00005
NM_017617.5(NOTCH1):c.2003C>T (p.Pro668Leu)	rs576030298	0.00003

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