ClinVar Miner

Submissions for variant NM_000245.4(MET):c.1701+58del

dbSNP: rs112241458
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 RCV001592670 SCV001823198 likely benign not provided 2019-08-30 criteria provided, single submitter clinical testing
Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital RCV002268532 SCV002550793 benign not specified 2023-08-15 criteria provided, single submitter clinical testing

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