ClinVar Miner

Submissions for variant NM_000051.4(ATM):c.6348-8T>A

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
MGZ Medical Genetics Center RCV002289377 SCV002580853 uncertain significance Familial cancer of breast 2022-06-03 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV003605782 SCV004437976 likely benign Ataxia-telangiectasia syndrome 2023-02-06 criteria provided, single submitter clinical testing

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