ClinVar Miner

Submissions for variant NM_000251.2(MSH2):c.108T>G (p.Leu36=) (rs876659034)

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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 RCV000219669 SCV000275002 likely benign Hereditary cancer-predisposing syndrome 2015-04-05 criteria provided, single submitter clinical testing
Invitae RCV000630305 SCV000751261 likely benign Hereditary nonpolyposis colorectal neoplasms 2017-10-17 criteria provided, single submitter clinical testing
Quest Diagnostics Nichols Institute San Juan Capistrano RCV000759094 SCV000888196 likely benign not provided 2018-08-01 criteria provided, single submitter clinical testing

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