ClinVar Miner

Submissions for variant NM_024652.6(LRRK1):c.4332+19T>G

gnomAD frequency: 0.00199  dbSNP: rs200705193
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002134443 SCV002456835 benign not provided 2025-01-16 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV002134443 SCV005293736 benign not provided criteria provided, single submitter not provided

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