ClinVar Miner

Submissions for variant NM_000051.4(ATM):c.7751_7754del (p.Thr2584fs)

dbSNP: rs2086308364
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Liquid Biopsy and Cancer Interception Group, Pfizer-University of Granada-Junta de Andalucía Centre for Genomics and Oncological Research RCV001090193 SCV001245490 pathogenic Familial cancer of breast criteria provided, single submitter clinical testing

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