ClinVar Miner

Submissions for variant NM_032043.2(BRIP1):c.1935+11G>A (rs79121306)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000410950 SCV000490031 likely benign Fanconi anemia, complementation group J 2016-10-04 criteria provided, single submitter clinical testing
Counsyl RCV000411701 SCV000490032 likely benign Neoplasm of ovary 2016-10-04 criteria provided, single submitter clinical testing
Color RCV000583266 SCV000689292 likely benign Hereditary cancer-predisposing syndrome 2016-02-25 criteria provided, single submitter clinical testing
PreventionGenetics,PreventionGenetics RCV000679778 SCV000807125 likely benign not provided 2017-06-08 criteria provided, single submitter clinical testing

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