ClinVar Miner

Variants with conflicting interpretations "benign" from Hereditary Cancer Genetics group, Vall d'Hebron Institute of Oncology and "likely benign" from any submitter

Minimum review status of the submission from Hereditary Cancer Genetics group, Vall d'Hebron Institute of Oncology: Collection method of the submission from Hereditary Cancer Genetics group, Vall d'Hebron Institute of Oncology:
Minimum review status of the other submission: Collection method of the other submission:
ClinVar version:
Total variants with conflicting interpretations: 8
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HGVS dbSNP gnomAD frequency
NM_007294.4(BRCA1):c.4113G>A (p.Gly1371=) rs147448807 0.00150
NM_000059.4(BRCA2):c.7435+6G>A rs81002852 0.00053
NM_000059.4(BRCA2):c.7805+13A>G rs149769332 0.00019
NM_000059.4(BRCA2):c.9501+4A>G rs81002848 0.00002
NM_007294.4(BRCA1):c.4485-10A>G rs863224420 0.00001
NM_000059.4(BRCA2):c.8488-20T>G rs1593930846
NM_007294.4(BRCA1):c.212+17T>C rs369461674
NM_007294.4(BRCA1):c.81-11T>C rs767144634

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