ClinVar Miner

Submissions for variant NM_005781.4(TNK2):c.2630G>A (p.Arg877His) (rs112384084)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Lupski Lab, Baylor-Hopkins CMG,Baylor College of Medicine RCV000210436 SCV000266505 likely pathogenic Parkinson disease 2016-01-01 criteria provided, single submitter research
PreventionGenetics RCV000254280 SCV000311272 benign not specified criteria provided, single submitter clinical testing

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