ClinVar Miner

Submissions for variant NM_000245.4(MET):c.2102+9A>T

gnomAD frequency: 0.00001  dbSNP: rs201495740
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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 RCV002135138 SCV002446937 likely benign Renal cell carcinoma 2022-02-10 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV005247580 SCV005899274 likely benign Papillary renal cell carcinoma type 1 2024-11-08 criteria provided, single submitter clinical testing This variant is considered likely benign. This variant is intronic and is not expected to impact mRNA splicing.

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