ClinVar Miner

Submissions for variant NM_014000.2(VCL):c.625A>T (p.Met209Leu) (rs144683137)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CHEO Genetics Diagnostic Laboratory,Children's Hospital of Eastern Ontario RCV000770294 SCV000901726 uncertain significance Cardiomyopathy 2015-11-06 criteria provided, single submitter clinical testing
Phosphorus, Inc. RCV000577945 SCV000679923 uncertain significance Dilated cardiomyopathy 1W 2017-08-01 criteria provided, single submitter clinical testing
Phosphorus, Inc. RCV000577975 SCV000679924 uncertain significance Familial hypertrophic cardiomyopathy 15 2017-08-01 criteria provided, single submitter clinical testing

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