ClinVar Miner

Variants with conflicting interpretations "pathogenic" from Genetics and Prenatal Diagnosis Center, The First Affiliated Hospital of Zhengzhou University and "uncertain significance" from Medical Cytogenetics and Molecular Genetics Laboratory, IRCCS Istituto Auxologico Italiano

Minimum review status of the submission from Genetics and Prenatal Diagnosis Center, The First Affiliated Hospital of Zhengzhou University: Collection method of the submission from Genetics and Prenatal Diagnosis Center, The First Affiliated Hospital of Zhengzhou University:
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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