ClinVar Miner

Variants with conflicting interpretations "likely benign" from GeneDx and "uncertain significance" from Service de Génétique Moléculaire, Hôpital Robert Debré

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_133379.5(TTN):c.16282G>A (p.Val5428Met) rs199565262 0.00010

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