ClinVar Miner

Submissions for variant NM_000314.7(PTEN):c.210-39A>G (rs370918174)

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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Cancer Genomic Medicine Translational Research Lab,Cleveland Clinic Genomic Medicine Institute RCV000516044 SCV000579250 uncertain significance Cowden syndrome 1 2017-05-26 no assertion criteria provided research
Color RCV000581383 SCV000691154 likely benign Hereditary cancer-predisposing syndrome 2015-01-20 criteria provided, single submitter clinical testing
PreventionGenetics RCV000249036 SCV000303571 likely benign not specified criteria provided, single submitter clinical testing
Quest Diagnostics Nichols Institute San Juan Capistrano RCV000249036 SCV000602116 likely benign not specified 2017-02-23 criteria provided, single submitter clinical testing
Quest Diagnostics Nichols Institute San Juan Capistrano RCV000759332 SCV000888590 benign not provided 2017-09-20 criteria provided, single submitter clinical testing

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