ClinVar Miner

Variants with conflicting interpretations "likely benign" from Evidence-based Network for the Interpretation of Germline Mutant Alleles (ENIGMA) and "benign" from DNA and Cytogenetics Diagnostics Unit,Erasmus Medical Center

Minimum review status of the submission from Evidence-based Network for the Interpretation of Germline Mutant Alleles (ENIGMA): Collection method of the submission from Evidence-based Network for the Interpretation of Germline Mutant Alleles (ENIGMA):
Minimum review status of the other submission: Collection method of the other submission:
ClinVar version:
Total variants with conflicting interpretations: 2
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HGVS dbSNP
NM_000059.3(BRCA2):c.6465C>T (p.Leu2155=) rs746099644
NM_007294.4(BRCA1):c.2733A>G (p.Gly911=) rs1800740

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