ClinVar Miner

Submissions for variant NM_000051.4(ATM):c.6452+7T>C

dbSNP: rs1555116551
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV000582862 SCV000687700 likely benign Hereditary cancer-predisposing syndrome 2017-07-18 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001448588 SCV001651683 likely benign Ataxia-telangiectasia syndrome 2023-04-06 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV004592867 SCV005083352 likely benign Familial cancer of breast 2024-06-06 criteria provided, single submitter clinical testing This variant is considered likely benign. This variant is intronic and is not expected to impact mRNA splicing.

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