ClinVar Miner

Submissions for variant NM_001370259.2(MEN1):c.784-129T>A

gnomAD frequency: 0.00001  dbSNP: rs536461697
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV002155423 SCV002419285 likely benign Multiple endocrine neoplasia, type 1 2022-10-25 criteria provided, single submitter clinical testing
Laboratory of Molecular and Cytogenetics, Department of Anatomy, All India Institute of Medical Sciences (AIIMS) RCV003233039 SCV003930417 benign Pituitary adenoma 5, multiple types 2023-05-10 criteria provided, single submitter research

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