ClinVar Miner

Submissions for variant NM_000535.7(PMS2):c.198T>C (p.Ile66=) (rs1554305014)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color RCV000582779 SCV000691052 likely benign Hereditary cancer-predisposing syndrome 2017-03-27 criteria provided, single submitter clinical testing
Invitae RCV000937688 SCV001083478 likely benign not provided 2018-05-17 criteria provided, single submitter clinical testing

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