ClinVar Miner

Submissions for variant NM_024652.6(LRRK1):c.1420-13CT[6]

dbSNP: rs373037498
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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 RCV002086023 SCV002386154 benign not provided 2024-12-15 criteria provided, single submitter clinical testing
PreventionGenetics, part of Exact Sciences RCV003911336 SCV004721059 likely benign LRRK1-related disorder 2020-08-03 no assertion criteria provided clinical testing This variant is classified as likely benign based on ACMG/AMP sequence variant interpretation guidelines (Richards et al. 2015 PMID: 25741868, with internal and published modifications).

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