ClinVar Miner

Submissions for variant NM_032043.2(BRIP1):c.380-24dup (rs545021924)

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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000160345 SCV000210851 benign Hereditary cancer-predisposing syndrome 2014-01-21 criteria provided, single submitter clinical testing The variant is found in BR-OV-HEREDIC,HEREDICANCER panel(s).
Counsyl RCV000411395 SCV000489877 likely benign Fanconi anemia, complementation group J 2016-06-27 criteria provided, single submitter clinical testing
Counsyl RCV000408968 SCV000489878 likely benign Neoplasm of ovary 2016-06-27 criteria provided, single submitter clinical testing
Color RCV000160345 SCV000684274 likely benign Hereditary cancer-predisposing syndrome 2015-04-07 criteria provided, single submitter clinical testing
PreventionGenetics,PreventionGenetics RCV000679788 SCV000807149 benign not specified 2017-02-17 criteria provided, single submitter clinical testing

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