ClinVar Miner

Submissions for variant NM_000179.2(MSH6):c.458-5del (rs587781955)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000130330 SCV000185180 likely benign Hereditary cancer-predisposing syndrome 2014-01-09 criteria provided, single submitter clinical testing
Invitae RCV000200208 SCV000253117 likely benign Lynch syndrome 2015-06-03 criteria provided, single submitter clinical testing
Invitae RCV000532572 SCV000624973 likely benign Hereditary nonpolyposis colon cancer 2019-12-31 criteria provided, single submitter clinical testing
Color RCV000130330 SCV001357798 likely benign Hereditary cancer-predisposing syndrome 2018-11-15 criteria provided, single submitter clinical testing

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