ClinVar Miner

Submissions for variant NM_007194.4(CHEK2):c.701_720del (p.Val234fs)

dbSNP: rs2145951528
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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 RCV001648489 SCV001852739 likely pathogenic Breast carcinoma 2021-09-10 no assertion criteria provided clinical testing

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