List of variants in gene combination LOC130003020, NOTCH1 reported as likely benign by GeneDx

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.-2G>A	rs921361590	0.00005
NM_017617.5(NOTCH1):c.-6G>T	rs1589085071
NM_017617.5(NOTCH1):c.17_18delinsTT (p.Ala6Val)	rs878855023
NM_017617.5(NOTCH1):c.51C>T (p.Leu17=)	rs1478932209

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