ClinVar Miner

Submissions for variant NM_000314.8(PTEN):c.795A>C (p.Leu265=)

dbSNP: rs891648600
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000645083 SCV000766825 likely benign PTEN hamartoma tumor syndrome 2021-07-17 criteria provided, single submitter clinical testing
Color Diagnostics, LLC DBA Color Health RCV000774652 SCV000908531 likely benign Hereditary cancer-predisposing syndrome 2018-05-15 criteria provided, single submitter clinical testing

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