ClinVar Miner

Submissions for variant NM_005591.4(MRE11):c.153+14G>C

gnomAD frequency: 0.00001  dbSNP: rs781257130
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002239162 SCV002509434 likely benign Ataxia-telangiectasia-like disorder 2024-05-02 criteria provided, single submitter clinical testing

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