Variants in gene NOD2 with conflicting interpretations "benign" and "uncertain significance"

Submission 1 (benign) minimum review status:		Submission 1 (benign) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) 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: 8

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HGVS	dbSNP	gnomAD frequency
NM_001370466.1(NOD2):c.2023C>T (p.Arg675Trp)	rs2066844	0.02936
NM_001370466.1(NOD2):c.2183C>T (p.Ala728Val)	rs61747625	0.00307
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.2474A>G (p.Asn825Ser)	rs104895467	0.00076
NM_001370466.1(NOD2):c.794C>T (p.Ala265Val)	rs149338478	0.00014
NM_001370466.1(NOD2):c.1753G>A (p.Ala585Thr)	rs104895438
NM_001370466.1(NOD2):c.2641G>T (p.Gly881Cys)	rs2066845

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