ClinVar Miner

Submissions for variant NM_000051.4(ATM):c.2466+87T>G

gnomAD frequency: 0.00304  dbSNP: rs145659155
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001530602 SCV001745485 likely benign not provided 2018-06-21 criteria provided, single submitter clinical testing
National Health Laboratory Service, Universitas Academic Hospital and University of the Free State RCV002225846 SCV002505317 benign Hereditary breast ovarian cancer syndrome 2022-04-19 criteria provided, single submitter clinical testing

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