ClinVar Miner

Variants in gene AXIN2 with conflicting interpretations "uncertain significance" and "benign"

Submission 1 (uncertain significance) minimum review status: Submission 1 (uncertain significance) method:
Submission 2 (benign) minimum review status: Submission 2 (benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 3
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NM_004655.4(AXIN2):c.1376G>A (p.Arg459His) rs368525111
NM_004655.4(AXIN2):c.1545C>T (p.His515=) rs139316692
NM_004655.4(AXIN2):c.270C>T (p.Asp90=) rs141655687

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