Variants in gene NOD2 with conflicting interpretations "likely benign" and "benign"

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) 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: 15

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HGVS	dbSNP	gnomAD frequency
NM_001370466.1(NOD2):c.2717+158C>T	rs5743289	0.10180
NM_001370466.1(NOD2):c.2782G>A (p.Val928Ile)	rs5743291	0.06122
NM_001370466.1(NOD2):c.2093C>G (p.Ala698Gly)	rs5743278	0.01319
NM_001370466.1(NOD2):c.1752C>T (p.Ala584=)	rs61736932	0.00840
NM_001370466.1(NOD2):c.785A>G (p.Asn262Ser)	rs5743271	0.00557
NM_001370466.1(NOD2):c.2183C>T (p.Ala728Val)	rs61747625	0.00307
NM_001370466.1(NOD2):c.485C>T (p.Thr162Met)	rs61755182	0.00291
NM_001370466.1(NOD2):c.2325G>T (p.Val775=)	rs104895495	0.00157
NM_001370466.1(NOD2):c.2296G>A (p.Val766Met)	rs104895444	0.00127
NM_001370466.1(NOD2):c.1211C>T (p.Ser404Leu)	rs104895431	0.00103
NM_001370466.1(NOD2):c.-8-7T>A	rs104895421	0.00092
NM_001370466.1(NOD2):c.552C>T (p.Ala184=)	rs5743269	0.00090
NM_001370466.1(NOD2):c.2474A>G (p.Asn825Ser)	rs104895467	0.00076
NM_001370466.1(NOD2):c.379G>A (p.Asp127Asn)	rs146054564	0.00068
NM_001370466.1(NOD2):c.1693G>A (p.Val565Met)	rs148683734	0.00041

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