ClinVar Miner

Submissions for variant NM_198578.4(LRRK2):c.6281-3dup

dbSNP: rs780258764
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000357757 SCV000378624 uncertain significance Autosomal dominant Parkinson disease 8 2016-06-14 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000357757 SCV004267357 benign Autosomal dominant Parkinson disease 8 2023-03-03 criteria provided, single submitter clinical testing

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