ClinVar Miner

Submissions for variant NM_000051.4(ATM):c.7308-11T>C

dbSNP: rs1565529149
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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 RCV000777382 SCV000913244 uncertain significance Hereditary cancer-predisposing syndrome 2018-07-21 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV003605689 SCV004501531 likely benign Ataxia-telangiectasia syndrome 2023-02-23 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV004588230 SCV005082941 likely benign Familial cancer of breast 2024-06-13 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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