ClinVar Miner

Submissions for variant NM_020975.6(RET):c.2076C>G (p.Ala692=)

dbSNP: rs1414025702
Minimum review status: Collection method:
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001880840 SCV002141637 likely benign Multiple endocrine neoplasia, type 2 2025-01-29 criteria provided, single submitter clinical testing

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