ClinVar Miner

Submissions for variant NM_005431.2(XRCC2):c.347_350del (p.Phe116fs)

dbSNP: rs764640893
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Medical Genetics Laboratory, Umraniye Training and Research Hospital, University of Health Sciences RCV001663392 SCV001877100 likely pathogenic Breast carcinoma no assertion criteria provided clinical testing

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