ClinVar Miner

Submissions for variant NM_014000.2(VCL):c.874+13T>C (rs777617736)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory for Molecular Medicine,Partners HealthCare Personalized Medicine RCV000600292 SCV000731529 likely benign not specified 2017-02-22 criteria provided, single submitter clinical testing c.874+13T>C in intron 7 of VCL: This variant is not expected to have clinical si gnificance because it is not located within the splice consensus sequence. It h as been identified in 3/11416 Latino chromosomes by the Exome Aggregation Consor tium (ExAC, http://exac.broadinstitute.org; dbSNP rs777617736).

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