ClinVar Miner

Variants with conflicting interpretations "likely benign" from ClinGen ENIGMA BRCA1 and BRCA2 Variant Curation Expert Panel, ClinGen and "uncertain significance" from any submitter

Minimum review status of the submission from ClinGen ENIGMA BRCA1 and BRCA2 Variant Curation Expert Panel, ClinGen: Collection method of the submission from ClinGen ENIGMA BRCA1 and BRCA2 Variant Curation Expert Panel, ClinGen:
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 gnomAD frequency
NM_000059.4(BRCA2):c.663T>G (p.Phe221Leu) rs80358891 0.00003
NM_000059.4(BRCA2):c.7008-5T>C rs397507380

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