ClinVar Miner

Submissions for variant NM_198578.4(LRRK2):c.-124G>C

gnomAD frequency: 0.04210  dbSNP: rs112643657
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000294489 SCV000483378 likely benign Autosomal dominant Parkinson disease 8 2016-06-14 criteria provided, single submitter clinical testing
GeneDx RCV001672742 SCV001884620 benign not provided 2018-08-17 criteria provided, single submitter clinical testing

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