Variants in gene NOD2 with conflicting interpretations "uncertain significance" and "risk factor"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (risk factor) minimum review status:		Submission 2 (risk factor) 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001370466.1(NOD2):c.2717+158C>T	rs5743289	0.10180
NM_001370466.1(NOD2):c.2023C>T (p.Arg675Trp)	rs2066844	0.02936
NM_001370466.1(NOD2):c.2641G>C (p.Gly881Arg)	rs2066845

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