ClinVar Miner

Submissions for variant NM_198578.4(LRRK2):c.347+2T>C

gnomAD frequency: 0.00084  dbSNP: rs141221000
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000596890 SCV000700750 uncertain significance not provided 2016-10-06 criteria provided, single submitter clinical testing
GeneDx RCV000596890 SCV001833517 benign not provided 2020-12-24 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002061995 SCV002333071 likely benign Autosomal dominant Parkinson disease 8 2024-11-05 criteria provided, single submitter clinical testing
Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Centre RCV002061995 SCV005442214 uncertain significance Autosomal dominant Parkinson disease 8 2024-12-19 criteria provided, single submitter clinical testing

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