ClinVar Miner

Submissions for variant NM_198578.4(LRRK2):c.4317+12del

gnomAD frequency: 0.01470  dbSNP: rs200829235
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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000359670 SCV000378607 likely benign Autosomal dominant Parkinson disease 8 2016-06-14 criteria provided, single submitter clinical testing
GeneDx RCV001579585 SCV001827605 benign not provided 2018-08-14 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000359670 SCV002357904 benign Autosomal dominant Parkinson disease 8 2025-02-03 criteria provided, single submitter clinical testing
Genome Diagnostics Laboratory, Amsterdam University Medical Center RCV001579585 SCV001807807 likely benign not provided no assertion criteria provided clinical testing
Genome Diagnostics Laboratory, University Medical Center Utrecht RCV001579585 SCV001928299 likely benign not provided no assertion criteria provided clinical testing

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