ClinVar Miner

Submissions for variant NM_000245.4(MET):c.1966-17T>C

gnomAD frequency: 0.00027  dbSNP: rs555288487
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
Labcorp Genetics (formerly Invitae), Labcorp RCV002117922 SCV002402637 benign Renal cell carcinoma 2024-01-04 criteria provided, single submitter clinical testing
Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital RCV002465922 SCV002760407 likely benign not specified 2023-08-15 criteria provided, single submitter clinical testing

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