ClinVar Miner

Submissions for variant NM_002878.3(RAD51D):c.481-7G>A (rs145832514)

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Total submissions: 8
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color RCV000580868 SCV000686460 likely benign Hereditary cancer-predisposing syndrome 2015-09-21 criteria provided, single submitter clinical testing
Counsyl RCV000204059 SCV000488984 likely benign Breast-ovarian cancer, familial 4 2016-07-29 criteria provided, single submitter clinical testing
EGL Genetic Diagnostics,Eurofins Clinical Diagnostics RCV000179411 SCV000231657 likely benign not specified 2015-01-07 criteria provided, single submitter clinical testing
GeneDx RCV000179411 SCV000171273 benign not specified 2014-04-01 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.
Integrated Genetics/Laboratory Corporation of America RCV000587972 SCV000698106 benign not provided 2016-02-15 criteria provided, single submitter clinical testing
Invitae RCV000204059 SCV000262322 benign Breast-ovarian cancer, familial 4 2017-12-29 criteria provided, single submitter clinical testing
Quest Diagnostics Nichols Institute San Juan Capistrano RCV000179411 SCV000602159 likely benign not specified 2017-02-14 criteria provided, single submitter clinical testing
Quest Diagnostics Nichols Institute San Juan Capistrano RCV000587972 SCV000889824 benign not provided 2018-06-20 criteria provided, single submitter clinical testing

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