ClinVar Miner

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

Submission 1 (likely benign) minimum review status: Submission 1 (likely benign) method:
Submission 2 (uncertain significance) minimum review status: Submission 2 (uncertain significance) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 10
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HGVS dbSNP
NM_001370466.1(NOD2):c.-8-7T>A rs104895421
NM_001370466.1(NOD2):c.1753G>A (p.Ala585Thr) rs104895438
NM_001370466.1(NOD2):c.2026C>T (p.Arg676Cys) rs5743277
NM_001370466.1(NOD2):c.2183C>T (p.Ala728Val) rs61747625
NM_001370466.1(NOD2):c.2291G>A (p.Arg764Gln) rs104895464
NM_001370466.1(NOD2):c.2296G>A (p.Val766Met) rs104895444
NM_001370466.1(NOD2):c.2641G>C (p.Gly881Arg) rs2066845
NM_001370466.1(NOD2):c.2938dup (p.Leu980fs) rs2066847
NM_001370466.1(NOD2):c.485C>T (p.Thr162Met) rs61755182
NM_001370466.1(NOD2):c.850C>T (p.Arg284Trp) rs104895427

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