ClinVar Miner

Submissions for variant NM_001370259.2(MEN1):c.1350+12C>A

gnomAD frequency: 0.00001  dbSNP: rs1186166424
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 RCV001994764 SCV002235714 likely benign Multiple endocrine neoplasia, type 1 2023-09-08 criteria provided, single submitter clinical testing

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