ClinVar Miner

Submissions for variant NM_058216.3(RAD51C):c.706-18T>C (rs56401264)

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Total submissions: 6
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000131016 SCV000185942 likely benign Hereditary cancer-predisposing syndrome 2015-03-19 criteria provided, single submitter clinical testing
Color RCV000131016 SCV000686376 benign Hereditary cancer-predisposing syndrome 2015-04-22 criteria provided, single submitter clinical testing
Counsyl RCV000409180 SCV000489815 likely benign Fanconi anemia, complementation group O 2016-06-09 criteria provided, single submitter clinical testing
Counsyl RCV000410295 SCV000489816 likely benign Breast-ovarian cancer, familial 3 2016-06-09 criteria provided, single submitter clinical testing
GeneDx RCV000212944 SCV000211613 benign not specified 2014-06-13 criteria provided, single submitter clinical testing This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease.
PreventionGenetics RCV000212944 SCV000807177 benign not specified 2018-01-08 criteria provided, single submitter clinical testing

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