ClinVar Miner

Submissions for variant NM_002878.3(RAD51D):c.234C>T (p.Ser78=) (rs9901455)

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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000162563 SCV000212974 benign Hereditary cancer-predisposing syndrome 2014-10-25 criteria provided, single submitter clinical testing General population or subpopulation frequency is too high to be a pathogenic mutation based on disease/syndrome prevalence and penetrance;Intronic alteration with no splicing impact by rt-pcr analysis or other splicing assay
PreventionGenetics,PreventionGenetics RCV000253532 SCV000309254 benign not specified criteria provided, single submitter clinical testing
EGL Genetic Diagnostics,Eurofins Clinical Diagnostics RCV000253532 SCV000335369 benign not specified 2015-09-11 criteria provided, single submitter clinical testing
Counsyl RCV000411810 SCV000488801 benign Breast-ovarian cancer, familial 4 2016-06-28 criteria provided, single submitter clinical testing
Color RCV000162563 SCV000537345 benign Hereditary cancer-predisposing syndrome 2015-03-31 criteria provided, single submitter clinical testing

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