ClinVar Miner

Submissions for variant NM_001370259.2(MEN1):c.183C>A (p.Leu61=)

dbSNP: rs1555166622
Minimum review status: Collection method:
Minimum conflict level:
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 RCV000632146 SCV000753251 likely benign Multiple endocrine neoplasia, type 1 2017-12-17 criteria provided, single submitter clinical testing

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