ClinVar Miner

Submissions for variant NM_000535.7(PMS2):c.2112C>T (p.Asp704=) (rs764735061)

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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 RCV000167092 SCV000217920 likely benign Hereditary cancer-predisposing syndrome 2014-12-09 criteria provided, single submitter clinical testing
Invitae RCV001089450 SCV000285104 likely benign Hereditary nonpolyposis colon cancer 2019-12-31 criteria provided, single submitter clinical testing
Integrated Genetics/Laboratory Corporation of America RCV000855561 SCV000697328 likely benign not specified 2019-08-29 criteria provided, single submitter clinical testing
Quest Diagnostics Nichols Institute San Juan Capistrano RCV000589117 SCV000889621 likely benign not provided 2017-11-16 criteria provided, single submitter clinical testing

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