ClinVar Miner

Submissions for variant NM_000051.4(ATM):c.5918+12T>C

dbSNP: rs2084042843
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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 RCV001185164 SCV001351319 likely benign Hereditary cancer-predisposing syndrome 2019-01-03 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002068405 SCV002395138 likely benign Ataxia-telangiectasia syndrome 2023-10-17 criteria provided, single submitter clinical testing

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