List of variants in gene NOTCH1 reported as uncertain significance by Institute for Clinical Genetics, University Hospital TU Dresden, University Hospital TU Dresden

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_017617.5(NOTCH1):c.2969+7G>A	rs770026189	0.00001
NM_017617.5(NOTCH1):c.3190G>A (p.Asp1064Asn)	rs375931404	0.00001
NM_017617.5(NOTCH1):c.2869G>C (p.Gly957Arg)	rs773902766
NM_017617.5(NOTCH1):c.5140A>G (p.Ile1714Val)	rs2133333190

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