ClinVar Miner

Submissions for variant NM_001142571.2(RAD51D):c.269A>G (p.Asp90Gly) (rs180869630)

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Total submissions: 7
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000127702 SCV000171281 benign not specified 2014-01-17 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.
Counsyl RCV000412012 SCV000488486 likely benign Breast-ovarian cancer, familial 4 2016-06-09 criteria provided, single submitter clinical testing
Color RCV000579452 SCV000686435 likely benign Hereditary cancer-predisposing syndrome 2015-01-20 criteria provided, single submitter clinical testing
Mendelics RCV000709446 SCV000839190 likely benign Hereditary breast and ovarian cancer syndrome 2018-07-02 criteria provided, single submitter clinical testing
Mendelics RCV000412012 SCV001140422 likely benign Breast-ovarian cancer, familial 4 2019-05-28 criteria provided, single submitter clinical testing
CeGaT Praxis fuer Humangenetik Tuebingen RCV000996524 SCV001151271 uncertain significance not provided 2017-04-01 criteria provided, single submitter clinical testing
True Health Diagnostics RCV000579452 SCV000788205 likely benign Hereditary cancer-predisposing syndrome 2018-02-27 no assertion criteria provided clinical testing

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