ClinVar Miner

Submissions for variant NM_014000.2(VCL):c.874+9C>G (rs756064535)

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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 RCV000215822 SCV000271188 likely benign not specified 2015-06-10 criteria provided, single submitter clinical testing c.874+9C>G in intron 7 of VCL: This variant is not expected to have clinical sig nificance because it is not located within the splice consensus sequence. It has been identified in 1/16342 South Asian chromosomes by the Exome Aggregation Con sortium (ExAC, http://exac.broadinstitute.org; dbSNP rs756064535).

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