ClinVar Miner

Submissions for variant NM_032043.2(BRIP1):c.1071A>G (p.Glu357=) (rs761017296)

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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 RCV000162831 SCV000213317 likely benign Hereditary cancer-predisposing syndrome 2015-12-09 criteria provided, single submitter clinical testing
Color RCV000162831 SCV000689242 likely benign Hereditary cancer-predisposing syndrome 2016-02-25 criteria provided, single submitter clinical testing
Invitae RCV000228755 SCV000290969 likely benign Familial cancer of breast; Fanconi anemia, complementation group J 2017-12-16 criteria provided, single submitter clinical testing

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