ClinVar Miner

Submissions for variant NM_000314.7(PTEN):c.585T>C (p.Phe195=) (rs1554900624)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000532309 SCV000645601 likely benign PTEN hamartoma tumor syndrome 2017-01-13 criteria provided, single submitter clinical testing
Color RCV000584148 SCV000691176 likely benign Hereditary cancer-predisposing syndrome 2016-02-23 criteria provided, single submitter clinical testing

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