ClinVar Miner

Submissions for variant NM_002878.3(RAD51D):c.494G>A (p.Arg165Gln) (rs4796033)

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Total submissions: 6
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV000756584 SCV000884439 benign not provided 2017-05-02 criteria provided, single submitter clinical testing
Ambry Genetics RCV000131069 SCV000185999 benign Hereditary cancer-predisposing syndrome 2014-11-19 criteria provided, single submitter clinical testing
Color RCV000131069 SCV000292088 benign Hereditary cancer-predisposing syndrome 2014-11-05 criteria provided, single submitter clinical testing
Counsyl RCV000409134 SCV000488799 benign Breast-ovarian cancer, familial 4 2016-06-18 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000289914 SCV000401967 likely benign Breast and Ovarian Cancer Susceptibility 2016-06-14 criteria provided, single submitter clinical testing
PreventionGenetics RCV000245575 SCV000309255 benign not specified criteria provided, single submitter clinical testing

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