ClinVar Miner

Submissions for variant NM_000051.4(ATM):c.3153+49C>T

gnomAD frequency: 0.00001  dbSNP: rs1221844555
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Total submissions: 2
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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 RCV001694190 SCV001906403 likely benign not provided no assertion criteria provided clinical testing
Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+ RCV001694190 SCV001959823 likely benign not provided no assertion criteria provided clinical testing

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