ClinVar Miner

Submissions for variant NM_000245.4(MET):c.2584-10_2584-9del

dbSNP: rs57349036
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001571682 SCV001796194 likely benign not provided 2019-08-30 criteria provided, single submitter clinical testing
Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital RCV002268520 SCV002550804 benign not specified 2025-03-04 criteria provided, single submitter clinical testing

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