ClinVar Miner

Submissions for variant NM_198578.4(LRRK2):c.*934_*936dup

dbSNP: rs367772598
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000259216 SCV000378651 uncertain significance Autosomal dominant Parkinson disease 8 2016-06-14 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004693106 SCV005191766 uncertain significance not provided criteria provided, single submitter not provided

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