ClinVar Miner

Submissions for variant NM_198578.4(LRRK2):c.7462+15G>C

gnomAD frequency: 0.00025  dbSNP: rs200420425
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002132638 SCV002438727 benign Autosomal dominant Parkinson disease 8 2023-12-25 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002132638 SCV002799172 likely benign Autosomal dominant Parkinson disease 8 2021-09-19 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004707779 SCV005230042 benign not provided criteria provided, single submitter not provided

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