ClinVar Miner

Variants with conflicting interpretations "uncertain significance" from Laboratoire de Genetique Moleculaire, Centre Hospitalier Universitaire de Bordeaux and "pathogenic" from Suna and Inan Kirac Foundation Neurodegeneration Research Laboratory, Koc University

Minimum review status of the submission from Laboratoire de Genetique Moleculaire, Centre Hospitalier Universitaire de Bordeaux: Collection method of the submission from Laboratoire de Genetique Moleculaire, Centre Hospitalier Universitaire de Bordeaux:
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
Single allele

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