ClinVar Miner

Submissions for variant NM_198578.4(LRRK2):c.2352C>A (p.Ser784Arg) (rs398124660)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Neurogenetic Laboratory,Oslo University Hospital RCV000082877 SCV000114940 uncertain significance Parkinson disease, late-onset 2014-01-22 no assertion criteria provided research

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