ClinVar Miner

Submissions for variant NM_000251.2(MSH2):c.2043A>G (p.Gln681=) (rs730881763)

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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000163402 SCV000213944 likely benign Hereditary cancer-predisposing syndrome 2014-09-25 criteria provided, single submitter clinical testing
Color RCV000163402 SCV000537428 likely benign Hereditary cancer-predisposing syndrome 2015-07-28 criteria provided, single submitter clinical testing
Invitae RCV000204609 SCV000262440 likely benign Hereditary nonpolyposis colon cancer 2017-11-11 criteria provided, single submitter clinical testing
PreventionGenetics RCV000679301 SCV000806021 likely benign not provided 2017-10-20 criteria provided, single submitter clinical testing
Quest Diagnostics Nichols Institute San Juan Capistrano RCV000507870 SCV000601451 uncertain significance not specified 2017-06-06 criteria provided, single submitter clinical testing

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