ClinVar Miner

Submissions for variant NM_000314.6(PTEN):c.802-3dupT (rs34003473)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
EGL Genetic Diagnostics,Eurofins Clinical Diagnostics RCV000180134 SCV000232521 benign not specified 2014-05-20 criteria provided, single submitter clinical testing
Invitae RCV000198551 SCV000252695 benign PTEN hamartoma tumor syndrome 2016-03-18 criteria provided, single submitter clinical testing

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