ClinVar Miner

Submissions for variant NM_000179.3(MSH6):c.4002-11_4002-10delinsA

dbSNP: rs1553333946
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000662832 SCV000785687 likely benign Lynch syndrome 5 2017-11-01 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV000662832 SCV004018464 uncertain significance Lynch syndrome 5 2023-03-27 criteria provided, single submitter clinical testing This variant is classified as a variant of uncertain significance as there is insufficient evidence to determine its impact on protein function and/or cancer risk.

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