ClinVar Miner

Submissions for variant NM_032043.2(BRIP1):c.1141-94G>T (rs114901675)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000411026 SCV000489845 benign Fanconi anemia, complementation group J 2016-06-08 criteria provided, single submitter clinical testing
Counsyl RCV000412056 SCV000489846 benign Neoplasm of ovary 2016-06-08 criteria provided, single submitter clinical testing
University of Washington Department of Laboratory Medicine, University of Washington RCV000209061 SCV000265037 likely benign Hereditary cancer-predisposing syndrome 2015-12-01 no assertion criteria provided clinical testing

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