ClinVar Miner

Submissions for variant NM_000245.4(MET):c.1701+14A>G

gnomAD frequency: 0.00003  dbSNP: rs768638354
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002163133 SCV002469956 likely benign Renal cell carcinoma 2023-12-03 criteria provided, single submitter clinical testing
Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital RCV003493921 SCV004243309 likely benign not specified 2024-02-06 criteria provided, single submitter clinical testing

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