ClinVar Miner

Submissions for variant NM_020975.6(RET):c.2742A>C (p.Pro914=)

dbSNP: rs375963128
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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 RCV001428427 SCV001631125 likely benign Multiple endocrine neoplasia, type 2 2019-05-30 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV001428427 SCV004838691 likely benign Multiple endocrine neoplasia, type 2 2023-02-24 criteria provided, single submitter clinical testing

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