ClinVar Miner

Submissions for variant NM_000251.2(MSH2):c.642A>G (p.Arg214=) (rs768931909)

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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001086577 SCV000261485 likely benign Hereditary nonpolyposis colorectal neoplasms 2019-12-31 criteria provided, single submitter clinical testing
Ambry Genetics RCV000213519 SCV000274162 likely benign Hereditary cancer-predisposing syndrome 2015-08-16 criteria provided, single submitter clinical testing
Quest Diagnostics Nichols Institute San Juan Capistrano RCV000205308 SCV001134371 benign not provided 2018-11-01 criteria provided, single submitter clinical testing
Color RCV000213519 SCV001350534 likely benign Hereditary cancer-predisposing syndrome 2019-03-04 criteria provided, single submitter clinical testing
Integrated Genetics/Laboratory Corporation of America RCV001193246 SCV001361974 likely benign not specified 2019-08-10 criteria provided, single submitter clinical testing

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