ClinVar Miner

Submissions for variant NM_007194.4(CHEK2):c.364_369del (p.Glu122_Tyr123del)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Biomedical Genomics and Oncogenetics Laboratory, Institut Pasteur de Tunis, University Tunis El Manar RCV003334410 SCV003919097 likely pathogenic Familial cancer of breast criteria provided, single submitter clinical testing

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