ClinVar Miner

Submissions for variant NM_198578.4(LRRK2):c.5948+8G>C

gnomAD frequency: 0.00001  dbSNP: rs756480297
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002078004 SCV002325883 likely benign Autosomal dominant Parkinson disease 8 2024-01-02 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV003395367 SCV004130564 likely benign not provided 2022-11-01 criteria provided, single submitter clinical testing LRRK2: BP4

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