ClinVar Miner

Variants in gene EDA with conflicting interpretations "likely benign" and "benign"

Submission 1 (likely benign) minimum review status: Submission 1 (likely benign) method:
Submission 2 (benign) minimum review status: Submission 2 (benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 5
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HGVS dbSNP gnomAD frequency
NM_001399.5(EDA):c.206G>T (p.Arg69Leu) rs132630309 0.00312
NM_001399.5(EDA):c.1001G>A (p.Arg334His) rs142948132 0.00042
NM_001399.5(EDA):c.464G>A (p.Arg155His) rs144403117 0.00026
NM_001399.5(EDA):c.390G>T (p.Gly130=) rs143746851 0.00012
NM_001399.5(EDA):c.1014G>A (p.Thr338=) rs750674219 0.00003

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