List of variants in gene NOTCH1 reported as pathogenic for hematologic disorder

Minimum submission review status:		Collection method:
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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.4129C>T (p.Pro1377Ser)	rs61751542	0.01511
NM_017617.5(NOTCH1):c.2296G>A (p.Gly766Ser)
NM_017617.5(NOTCH1):c.4775T>G (p.Phe1592Cys)	rs796065341

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