Variants in gene NOTCH2 with conflicting interpretations "benign" and "likely benign"

Submission 1 (benign) minimum review status:		Submission 1 (benign) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely 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
NM_024408.4(NOTCH2):c.3441G>A (p.Glu1147=)	rs371875533
NM_024408.4(NOTCH2):c.3625T>G (p.Phe1209Val)	rs147223770
NM_024408.4(NOTCH2):c.4238T>A (p.Leu1413His)	rs41313282
NM_024408.4(NOTCH2):c.6094C>A (p.His2032Asn)	rs143236410
NM_024408.4(NOTCH2):c.6223G>A (p.Val2075Met)	rs150516342

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