ClinVar Miner

Submissions for variant NM_000314.8(PTEN):c.993C>T (p.Asp331=)

dbSNP: rs2132283468
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002086793 SCV002323531 likely benign PTEN hamartoma tumor syndrome 2021-03-02 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV003155463 SCV003844553 likely benign not specified 2023-02-02 criteria provided, single submitter clinical testing

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