ClinVar Miner

Submissions for variant NM_198578.4(LRRK2):c.5467C>A (p.Gln1823Lys)

gnomAD frequency: 0.00024  dbSNP: rs72547980
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000032484 SCV002423062 likely benign Autosomal dominant Parkinson disease 8 2023-10-23 criteria provided, single submitter clinical testing
GeneReviews RCV000032484 SCV000056145 not provided Autosomal dominant Parkinson disease 8 no assertion provided literature only

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