ClinVar Miner

Submissions for variant NM_005591.4(MRE11):c.1564-15TCT[4]

dbSNP: rs761058908
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002239110 SCV002509587 likely benign Ataxia-telangiectasia-like disorder 2021-03-09 criteria provided, single submitter clinical testing
Sema4, Sema4 RCV002258397 SCV002538397 likely benign Hereditary cancer-predisposing syndrome 2021-01-01 criteria provided, single submitter curation

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