ClinVar Miner

Submissions for variant NM_000245.4(MET):c.1528-13C>A

gnomAD frequency: 0.00004  dbSNP: rs751613983
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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 RCV002170730 SCV002348082 likely benign Renal cell carcinoma 2023-09-08 criteria provided, single submitter clinical testing
Sema4, Sema4 RCV002259158 SCV002532104 uncertain significance Hereditary cancer-predisposing syndrome 2022-02-19 criteria provided, single submitter curation

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