ClinVar Miner

Submissions for variant NM_001304718.2(PTEN):c.-362del (rs121913292)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Pathway Genomics RCV000172822 SCV000223788 pathogenic Cowden syndrome 1 2014-10-30 criteria provided, single submitter clinical testing
HudsonAlpha Institute for Biotechnology, HudsonAlpha Institute for Biotechnology RCV000172822 SCV001190317 pathogenic Cowden syndrome 1 2019-12-06 criteria provided, single submitter research

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