ClinVar Miner

Submissions for variant NM_000059.3(BRCA2):c.905C>G (p.Thr302Ser) (rs80359158)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Breast Cancer Information Core (BIC) (BRCA2) RCV000112862 SCV000145787 uncertain significance Breast-ovarian cancer, familial 2 2004-02-20 no assertion criteria provided clinical testing
Color RCV000773257 SCV000906882 uncertain significance Hereditary cancer-predisposing syndrome 2018-10-18 criteria provided, single submitter clinical testing
Quest Diagnostics Nichols Institute San Juan Capistrano RCV000758970 SCV000887955 uncertain significance not provided 2017-10-27 criteria provided, single submitter clinical testing

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