ClinVar Miner

Submissions for variant NM_014000.3(VCL):c.3153+47T>C

gnomAD frequency: 0.42070  dbSNP: rs2270550
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001675033 SCV001886795 benign not provided 2019-08-15 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV002243388 SCV002514452 benign Hypertrophic cardiomyopathy 15 2021-12-05 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001675033 SCV005315868 benign not provided criteria provided, single submitter not provided

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