ClinVar Miner

Submissions for variant NM_000179.2(MSH6):c.3642A>G (p.Glu1214=) (rs765247025)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000566298 SCV000662351 likely benign Hereditary cancer-predisposing syndrome 2015-03-25 criteria provided, single submitter clinical testing
Color RCV000566298 SCV000690381 likely benign Hereditary cancer-predisposing syndrome 2017-03-29 criteria provided, single submitter clinical testing
Invitae RCV000630257 SCV000751213 likely benign Hereditary nonpolyposis colon cancer 2017-08-29 criteria provided, single submitter clinical testing

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