ClinVar Miner

Submissions for variant NM_020975.6(RET):c.381G>C (p.Leu127=)

dbSNP: rs2132678686
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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 RCV002150224 SCV002412963 likely benign Multiple endocrine neoplasia, type 2 2025-01-10 criteria provided, single submitter clinical testing

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