ClinVar Miner

Submissions for variant NM_001081.4(CUBN):c.6916T>C (p.Trp2306Arg)

gnomAD frequency: 0.00002  dbSNP: rs1322005237
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Mayo Clinic Laboratories, Mayo Clinic RCV003481964 SCV004225212 uncertain significance not provided 2022-03-04 criteria provided, single submitter clinical testing BP4, PM2

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