ClinVar Miner

Submissions for variant NM_000059.3(BRCA2):c.8447G>C (p.Gly2816Ala) (rs56096120)

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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 RCV000210908 SCV000264594 uncertain significance Hereditary breast and ovarian cancer syndrome 2015-12-01 criteria provided, single submitter research
Sharing Clinical Reports Project (SCRP) RCV000238816 SCV000297567 uncertain significance Breast-ovarian cancer, familial 2 2012-12-28 no assertion criteria provided clinical testing

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