List of variants in gene NOTCH1 reported as uncertain significance by Clinical Molecular Genetics Laboratory, Johns Hopkins All Children's Hospital

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.4898G>A (p.Arg1633His)	rs375018022	0.00064
NM_017617.5(NOTCH1):c.4168C>A (p.Pro1390Thr)	rs191645600	0.00061
NM_017617.5(NOTCH1):c.2458C>T (p.Pro820Ser)	rs1379596542	0.00003

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