ClinVar Miner

Submissions for variant NM_001370259.2(MEN1):c.984C>T (p.His328=)

gnomAD frequency: 0.00001  dbSNP: rs757323408
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 RCV000938389 SCV001084198 likely benign Multiple endocrine neoplasia, type 1 2024-06-25 criteria provided, single submitter clinical testing

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