ClinVar Miner

Submissions for variant NM_014000.3(VCL):c.168+9G>T

dbSNP: rs997516030
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine RCV000602642 SCV000712282 likely benign not specified 2016-06-24 criteria provided, single submitter clinical testing c.168+9G>T in intron 1 of VCL: This variant is not expected to have clinical sig nificance because it is not located within the splice consensus sequence.
Labcorp Genetics (formerly Invitae), Labcorp RCV002062133 SCV002487580 likely benign Dilated cardiomyopathy 1W 2024-10-15 criteria provided, single submitter clinical testing
Clinical Genetics, Academic Medical Center RCV000602642 SCV001979017 benign not specified no assertion criteria provided clinical testing
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center RCV001729650 SCV001980533 likely benign not provided no assertion criteria provided clinical testing

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