ClinVar Miner

Submissions for variant NM_005591.4(MRE11):c.678T>C (p.Thr226=)

dbSNP: rs2135047870
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV002239137 SCV002509581 likely benign Ataxia-telangiectasia-like disorder 2021-04-09 criteria provided, single submitter clinical testing

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