ClinVar Miner

Submissions for variant NM_000179.3(MSH6):c.3646+18_3646+19delinsAA

dbSNP: rs1669977633
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV001187627 SCV001354480 likely benign Hereditary cancer-predisposing syndrome 2016-07-20 criteria provided, single submitter clinical testing

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