ClinVar Miner

Submissions for variant NM_198578.4(LRRK2):c.4883G>A (p.Arg1628His)

dbSNP: rs33949390
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Center for Human Genetics Tuebingen RCV000658642 SCV000780424 uncertain significance not provided 2018-03-01 criteria provided, single submitter clinical testing
Invitae RCV000699356 SCV000828062 likely benign Autosomal dominant Parkinson disease 8 2023-05-12 criteria provided, single submitter clinical testing
Mendelics RCV000699356 SCV001138690 uncertain significance Autosomal dominant Parkinson disease 8 2019-05-28 criteria provided, single submitter clinical testing
Revvity Omics, Revvity RCV000658642 SCV004236278 uncertain significance not provided 2019-11-25 criteria provided, single submitter clinical testing

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