ClinVar Miner

Submissions for variant NM_000314.8(PTEN):c.1027-6C>A

dbSNP: rs1374474745
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV001192233 SCV001360260 uncertain significance Hereditary cancer-predisposing syndrome 2019-01-31 criteria provided, single submitter clinical testing
Invitae RCV003619740 SCV004459281 likely benign PTEN hamartoma tumor syndrome 2023-04-27 criteria provided, single submitter clinical testing

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