ClinVar Miner

Submissions for variant NM_000051.4(ATM):c.2124+21A>G

gnomAD frequency: 0.00004  dbSNP: rs770563728
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Clinical Genetics Laboratory, Department of Pathology, Netherlands Cancer Institute RCV001694189 SCV001906402 likely benign not provided no assertion criteria provided clinical testing
Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+ RCV001694189 SCV001954823 likely benign not provided no assertion criteria provided clinical testing
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center RCV001694189 SCV001980346 likely benign not provided no assertion criteria provided clinical testing

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