ClinVar Miner

Variants with conflicting interpretations "uncertain significance" from GeneDx and "pathogenic" from Codex Genetics Limited

Minimum review status of the submission from GeneDx: Collection method of the submission from GeneDx:
Minimum review status of the other submission: Collection method of the other submission:
ClinVar version:
Total variants with conflicting interpretations: 1
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HGVS dbSNP gnomAD frequency
NM_002693.3(POLG):c.2890C>T (p.Arg964Cys) rs201477273 0.00033

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