ClinVar Miner

Submissions for variant NM_000245.4(MET):c.-207C>G

gnomAD frequency: 0.39920  dbSNP: rs1858830
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001515284 SCV001723320 benign Renal cell carcinoma 2024-01-18 criteria provided, single submitter clinical testing
GeneDx RCV001673089 SCV001886325 benign not provided 2018-06-23 criteria provided, single submitter clinical testing This variant is associated with the following publications: (PMID: 17053076, 24150225, 24909855, 23097380, 19681062)
Breakthrough Genomics, Breakthrough Genomics RCV001673089 SCV005273274 benign not provided criteria provided, single submitter not provided

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