ClinVar Miner

Submissions for variant NM_000059.3(BRCA2):c.3395A>G (p.Lys1132Arg) (rs80358582)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000218723 SCV000276791 uncertain significance Hereditary cancer-predisposing syndrome 2015-06-30 criteria provided, single submitter clinical testing
Breast Cancer Information Core (BIC) (BRCA2) RCV000031419 SCV000146223 uncertain significance Breast-ovarian cancer, familial 2 2003-12-23 no assertion criteria provided clinical testing
Sharing Clinical Reports Project (SCRP) RCV000031419 SCV000054024 uncertain significance Breast-ovarian cancer, familial 2 2007-12-13 no assertion criteria provided clinical testing

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