Variants in gene NOTCH2 with conflicting interpretations "uncertain significance" and "benign"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (benign) minimum review status:		Submission 2 (benign) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 5

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HGVS	dbSNP	gnomAD frequency
NM_024408.4(NOTCH2):c.7223T>A (p.Leu2408His)	rs35586704	0.00228
NM_024408.4(NOTCH2):c.2830G>T (p.Asp944Tyr)	rs151130105	0.00067
NM_024408.4(NOTCH2):c.423G>A (p.Glu141=)	rs149906722	0.00058
NM_024408.4(NOTCH2):c.6363G>C (p.Lys2121Asn)	rs144047610	0.00050
NM_024408.4(NOTCH2):c.15C>G (p.Arg5=)	rs4021006

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