ClinVar Miner

Submissions for variant NM_000179.3(MSH6):c.3439-8A>G

dbSNP: rs863224332
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV001186604 SCV001353078 likely benign Hereditary cancer-predisposing syndrome 2018-11-06 criteria provided, single submitter clinical testing
Invitae RCV001393073 SCV001594726 likely benign Hereditary nonpolyposis colorectal neoplasms 2020-08-22 criteria provided, single submitter clinical testing
Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital RCV003320594 SCV004024803 likely benign not specified 2023-08-15 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV003996954 SCV004815884 likely benign Lynch syndrome 2023-02-24 criteria provided, single submitter clinical testing

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