ClinVar Miner

Variants with conflicting interpretations "pathogenic" from Institut de Recherche Interdisciplinaire en Biologie Humaine et Moleculaire, Universite Libre de Bruxelles and "likely pathogenic" from Service de Génétique Moléculaire, Hôpital Robert Debré

Minimum review status of the submission from Institut de Recherche Interdisciplinaire en Biologie Humaine et Moleculaire, Universite Libre de Bruxelles: Collection method of the submission from Institut de Recherche Interdisciplinaire en Biologie Humaine et Moleculaire, Universite Libre de Bruxelles:
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_018136.5(ASPM):c.6686_6689del (p.Arg2229fs) rs770540184

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