ClinVar Miner

Submissions for variant NM_000314.7(PTEN):c.*10dup (rs756681683)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000662795 SCV000785611 uncertain significance Cowden syndrome 1 2017-10-10 criteria provided, single submitter clinical testing
Color RCV000771455 SCV000903862 likely benign Hereditary cancer-predisposing syndrome 2016-03-06 criteria provided, single submitter clinical testing

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