ClinVar Miner

Submissions for variant NM_001370259.2(MEN1):c.762_768dup (p.Leu257fs)

dbSNP: rs1555165488
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
Center for Human Genetics, University of Leuven RCV000664332 SCV000606806 likely pathogenic Multiple endocrine neoplasia, type 1 2017-10-06 criteria provided, single submitter clinical testing

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