ClinVar Miner

Submissions for variant NM_001370259.2(MEN1):c.446-11C>G

gnomAD frequency: 0.00001  dbSNP: rs1273035105
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 RCV002112622 SCV002400555 likely benign Multiple endocrine neoplasia, type 1 2025-01-19 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV002112622 SCV004828878 likely benign Multiple endocrine neoplasia, type 1 2023-07-10 criteria provided, single submitter clinical testing

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