ClinVar Miner

Submissions for variant NM_002878.3(RAD51D):c.198G>T (p.Val66=) (rs200810304)

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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 RCV000163761 SCV000214339 likely benign Hereditary cancer-predisposing syndrome 2015-01-12 criteria provided, single submitter clinical testing
Counsyl RCV000411752 SCV000488844 likely benign Breast-ovarian cancer, familial 4 2016-07-05 criteria provided, single submitter clinical testing
GeneDx RCV000425576 SCV000514355 likely benign not specified 2016-02-02 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.
Color RCV000163761 SCV000537457 likely benign Hereditary cancer-predisposing syndrome 2015-07-15 criteria provided, single submitter clinical testing
Invitae RCV000411752 SCV000561575 likely benign Breast-ovarian cancer, familial 4 2019-12-31 criteria provided, single submitter clinical testing
Integrated Genetics/Laboratory Corporation of America RCV000425576 SCV001338661 likely benign not specified 2020-04-23 criteria provided, single submitter clinical testing

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