ClinVar Miner

Submissions for variant NM_198578.4(LRRK2):c.6844-9_6844-8dup

dbSNP: rs72546334
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001562689 SCV001785493 likely benign not provided 2019-09-20 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002072134 SCV002406395 benign Autosomal dominant Parkinson disease 8 2025-01-11 criteria provided, single submitter clinical testing

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