ClinVar Miner

Submissions for variant NM_000051.4(ATM):c.6808-6T>C

dbSNP: rs995574419
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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 RCV000583200 SCV000687729 likely benign Hereditary cancer-predisposing syndrome 2017-04-24 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV004592872 SCV005085682 likely benign Familial cancer of breast 2024-06-12 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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