ClinVar Miner

Submissions for variant NM_020975.6(RET):c.639C>A (p.Pro213=)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
All of Us Research Program, National Institutes of Health RCV004807844 SCV005430299 likely benign Multiple endocrine neoplasia, type 2 2024-08-13 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV004807844 SCV005753421 likely benign Multiple endocrine neoplasia, type 2 2024-05-05 criteria provided, single submitter clinical testing

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