ClinVar Miner

Variants in gene EGR2 with conflicting interpretations "uncertain significance" and "likely benign"

Submission 1 (uncertain significance) minimum review status: Submission 1 (uncertain significance) method:
Submission 2 (likely benign) minimum review status: Submission 2 (likely benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 8
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NM_000399.5(EGR2):c.108G>A (p.Val36=) rs746579337
NM_000399.5(EGR2):c.1352G>T (p.Gly451Val) rs138967272
NM_000399.5(EGR2):c.1399G>C (p.Ala467Pro) rs146116229
NM_000399.5(EGR2):c.192G>C (p.Met64Ile) rs146631014
NM_000399.5(EGR2):c.457A>C (p.Thr153Pro) rs202183386
NM_000399.5(EGR2):c.644C>T (p.Thr215Met) rs139147487
NM_000399.5(EGR2):c.832G>A (p.Ala278Thr) rs565355765
NM_000399.5(EGR2):c.897AGC[6] (p.Ala309dup) rs746688326

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