ClinVar Miner

Submissions for variant NM_000051.4(ATM):c.3284+20T>C

dbSNP: rs1448789912
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV001181183 SCV001346281 likely benign Hereditary cancer-predisposing syndrome 2018-12-14 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002558994 SCV003461237 likely benign Ataxia-telangiectasia syndrome 2023-01-06 criteria provided, single submitter clinical testing

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