ClinVar Miner

Submissions for variant NM_000051.4(ATM):c.1803-15T>C

dbSNP: rs2080225396
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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 RCV001181155 SCV001346249 likely benign Hereditary cancer-predisposing syndrome 2018-10-09 criteria provided, single submitter clinical testing
Invitae RCV002558991 SCV002956064 likely benign Ataxia-telangiectasia syndrome 2023-08-28 criteria provided, single submitter clinical testing

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