ClinVar Miner

Submissions for variant NM_001370259.2(MEN1):c.913-65_913-14del

dbSNP: rs1555165154
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
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV000506209 SCV000604208 uncertain significance not specified 2016-11-16 criteria provided, single submitter clinical testing

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