ClinVar Miner

Submissions for variant NM_007294.4(BRCA1):c.4358-2786G>A

gnomAD frequency: 0.00003  dbSNP: rs374435098
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CSER _CC_NCGL, University of Washington RCV000149888 SCV000196736 likely pathogenic Hereditary breast ovarian cancer syndrome 2014-06-01 criteria provided, single submitter research
All of Us Research Program, National Institutes of Health RCV003998181 SCV004826806 likely benign Breast-ovarian cancer, familial, susceptibility to, 1 2023-04-28 criteria provided, single submitter clinical testing

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