ClinVar Miner

Submissions for variant NM_020975.6(RET):c.2382C>T (p.Cys794=)

dbSNP: rs1554819412
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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 RCV000532454 SCV000658448 likely benign Multiple endocrine neoplasia, type 2 2017-01-15 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV000532454 SCV005430378 likely benign Multiple endocrine neoplasia, type 2 2024-07-20 criteria provided, single submitter clinical testing

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