ClinVar Miner

Submissions for variant NM_198578.3(LRRK2):c.7153G>A (p.Gly2385Arg) (rs34778348)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneReviews RCV000032508 SCV000056171 pathologic Parkinson disease 8, autosomal dominant 2012-09-13 no assertion criteria provided curation Converted during submission to Pathogenic.
Illumina Clinical Services Laboratory,Illumina RCV000032508 SCV000378631 likely benign Parkinson disease 8, autosomal dominant 2016-06-14 criteria provided, single submitter clinical testing
OMIM RCV000032508 SCV000022178 risk factor Parkinson disease 8, autosomal dominant 2008-10-01 no assertion criteria provided literature only

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