ClinVar Miner

Submissions for variant NM_000314.7(PTEN):c.759C>T (p.Ile253=) (rs752250585)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000469547 SCV000554538 likely benign PTEN hamartoma tumor syndrome 2017-11-30 criteria provided, single submitter clinical testing
Ambry Genetics RCV000491272 SCV000580042 likely benign Hereditary cancer-predisposing syndrome 2012-06-05 criteria provided, single submitter clinical testing
Color RCV000491272 SCV000686301 likely benign Hereditary cancer-predisposing syndrome 2017-05-04 criteria provided, single submitter clinical testing

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