ClinVar Miner

Submissions for variant NM_058216.3(RAD51C):c.336G>A (p.Gly112=) (rs746122031)

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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000162688 SCV000213142 likely benign Hereditary cancer-predisposing syndrome 2015-01-19 criteria provided, single submitter clinical testing
Invitae RCV000206258 SCV000261961 likely benign Fanconi anemia, complementation group O 2019-12-31 criteria provided, single submitter clinical testing
Counsyl RCV000206258 SCV000490055 likely benign Fanconi anemia, complementation group O 2016-10-19 criteria provided, single submitter clinical testing
Counsyl RCV000409818 SCV000490056 likely benign Breast-ovarian cancer, familial 3 2016-10-19 criteria provided, single submitter clinical testing
Color RCV000162688 SCV000686341 likely benign Hereditary cancer-predisposing syndrome 2017-01-25 criteria provided, single submitter clinical testing

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