ClinVar Miner

Submissions for variant NM_198578.4(LRRK2):c.*131del

dbSNP: rs572544182
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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 RCV000341784 SCV000378638 uncertain significance Autosomal dominant Parkinson disease 8 2016-06-14 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV002292518 SCV002585389 benign not provided 2022-08-01 criteria provided, single submitter clinical testing LRRK2: BS1, BS2

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