ClinVar Miner

Submissions for variant NM_000051.4(ATM):c.2124+12dup

dbSNP: rs769051992
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001516185 SCV001724423 benign Ataxia-telangiectasia syndrome 2023-11-30 criteria provided, single submitter clinical testing
Color Diagnostics, LLC DBA Color Health RCV003584973 SCV004357185 likely benign Hereditary cancer-predisposing syndrome 2018-08-21 criteria provided, single submitter clinical testing

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