ClinVar Miner

Submissions for variant NM_000051.4(ATM):c.1803-9T>C

dbSNP: rs2135352230
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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 RCV001465481 SCV001669469 likely benign Ataxia-telangiectasia syndrome 2019-04-26 criteria provided, single submitter clinical testing
Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital RCV004596460 SCV005090047 likely benign not specified 2025-03-04 criteria provided, single submitter clinical testing

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