ClinVar Miner

Submissions for variant NM_017882.3(CLN6):c.601A>G (p.Lys201Glu) (rs587780316)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory, University of Chicago RCV000116760 SCV000150736 uncertain significance not provided 2014-01-24 criteria provided, single submitter clinical testing
Athena Diagnostics Inc RCV000517586 SCV000612847 uncertain significance not specified 2017-06-23 criteria provided, single submitter clinical testing
Counsyl RCV000667213 SCV000791631 uncertain significance Neuronal ceroid lipofuscinosis 6 2017-05-19 criteria provided, single submitter clinical testing

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