ClinVar Miner

Submissions for variant NM_005591.4(MRE11):c.1225+23G>T

gnomAD frequency: 0.00631  dbSNP: rs139950536
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001652630 SCV001865780 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
National Health Laboratory Service, Universitas Academic Hospital and University of the Free State RCV002225897 SCV002504813 likely benign Hereditary breast ovarian cancer syndrome 2022-04-19 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001652630 SCV005213260 likely benign not provided criteria provided, single submitter not provided

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