ClinVar Miner

Submissions for variant NM_198578.4(LRRK2):c.7155A>G (p.Gly2385=) (rs33962975)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Athena Diagnostics Inc RCV000712243 SCV000842688 benign not provided 2017-08-11 criteria provided, single submitter clinical testing
GeneReviews RCV000032509 SCV000056172 unknown Parkinson disease 8, autosomal dominant 2012-09-13 no assertion criteria provided curation Converted during submission to Uncertain significance.
Illumina Clinical Services Laboratory,Illumina RCV000032509 SCV000378632 likely benign Parkinson disease 8, autosomal dominant 2016-06-14 criteria provided, single submitter clinical testing

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