ClinVar Miner

Submissions for variant NM_000245.4(MET):c.1701+7A>T

gnomAD frequency: 0.00001  dbSNP: rs749081367
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000525266 SCV000623388 benign Renal cell carcinoma 2024-01-27 criteria provided, single submitter clinical testing

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