ClinVar Miner

Submissions for variant NM_001370259.2(MEN1):c.159C>T (p.Val53=)

dbSNP: rs1411927545
Minimum review status: Collection method:
Minimum conflict level:
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 RCV001407849 SCV001609831 likely benign Multiple endocrine neoplasia, type 1 2024-07-23 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004704351 SCV005211259 likely benign not provided criteria provided, single submitter not provided

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