ClinVar Miner

Submissions for variant NM_001370259.2(MEN1):c.1158C>G (p.Gly386=)

dbSNP: rs794728653
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001401970 SCV001603810 likely benign Multiple endocrine neoplasia, type 1 2022-05-17 criteria provided, single submitter clinical testing

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