ClinVar Miner

Submissions for variant NM_198578.4(LRRK2):c.4537-6T>C

gnomAD frequency: 0.00001  dbSNP: rs779382508
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001520584 SCV001729717 benign Autosomal dominant Parkinson disease 8 2023-12-11 criteria provided, single submitter clinical testing

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