ClinVar Miner

Variants with conflicting interpretations "uncertain significance" from Department of Medical Genetics, University Hospital of North Norway and "likely benign" from Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center

Minimum review status of the submission from Department of Medical Genetics, University Hospital of North Norway: Collection method of the submission from Department of Medical Genetics, University Hospital of North Norway:
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_007294.4(BRCA1):c.3708T>G (p.Asn1236Lys) rs28897687 0.00031

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