ClinVar Miner

Submissions for variant NM_000314.8(PTEN):c.209+84G>A

gnomAD frequency: 0.00199  dbSNP: rs185262832
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Mendelics RCV000988413 SCV001138125 likely benign PTEN hamartoma tumor syndrome 2019-05-28 criteria provided, single submitter clinical testing
GeneDx RCV001644871 SCV001857233 benign not provided 2015-03-03 criteria provided, single submitter clinical testing

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