ClinVar Miner

Variants with conflicting interpretations "uncertain significance" from Evidence-based Network for the Interpretation of Germline Mutant Alleles (ENIGMA) and "likely pathogenic" from Sharing Clinical Reports Project (SCRP)

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: 1
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HGVS dbSNP
NM_007294.3(BRCA1):c.4096+3A>G rs80358015

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