ClinVar Miner

Submissions for variant NM_001370259.2(MEN1):c.1560G>A (p.Gly520=)

dbSNP: rs969035156
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 RCV002194046 SCV002482664 likely benign Multiple endocrine neoplasia, type 1 2024-11-26 criteria provided, single submitter clinical testing

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