ClinVar Miner

Submissions for variant NM_000179.3(MSH6):c.4001+16T>A

gnomAD frequency: 0.00002  dbSNP: rs775091710
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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 RCV001184658 SCV001350685 likely benign Hereditary cancer-predisposing syndrome 2018-12-05 criteria provided, single submitter clinical testing
GeneDx RCV001712875 SCV001940743 benign not provided 2015-09-09 criteria provided, single submitter clinical testing
Invitae RCV002068390 SCV002399672 likely benign Hereditary nonpolyposis colorectal neoplasms 2023-10-22 criteria provided, single submitter clinical testing

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