ClinVar Miner

Submissions for variant NM_058216.3(RAD51C):c.870T>A (p.Ile290=) (rs376402418)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000163858 SCV000214445 likely benign Hereditary cancer-predisposing syndrome 2014-08-15 criteria provided, single submitter clinical testing
Color RCV000163858 SCV000686397 likely benign Hereditary cancer-predisposing syndrome 2015-08-17 criteria provided, single submitter clinical testing
Invitae RCV000204484 SCV000261035 likely benign Fanconi anemia, complementation group O 2017-12-11 criteria provided, single submitter clinical testing
Mendelics RCV000709515 SCV000839339 uncertain significance Hereditary breast and ovarian cancer syndrome 2018-07-02 criteria provided, single submitter clinical testing

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