ClinVar Miner

List of variants in gene NOTCH1 reported as uncertain significance by Genetics and Molecular Pathology, SA Pathology

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_017617.5(NOTCH1):c.6521A>G (p.Lys2174Arg)	rs761602495	0.00004
NM_017617.5(NOTCH1):c.2372A>G (p.Asn791Ser)	rs2133358146

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