120-association public preview gene page
LRRK2
leucine rich repeat kinase 2
Release Packages
Methods and glossaryrelease directory Git tag Data dictionary integrity.json ZIP archive
Identity
genes.json- Symbol
- LRRK2
- Name
- leucine rich repeat kinase 2
- Aliases
- DKFZp434H2111, FLJ45829, PARK8, RIPK7, ROCO2
- Provenance
- ClinVar, HGNC, Open Targets Platform
Parkinson disease
assoc:18618:0005180:2c2dffd3b9c0 · parkinson-top120-v0.1.0-preview
- Status
- observed unreviewed
- Support tier
- multi source observed
- Review
- automatic checks only
- Max source-reported score
- 0.880
Source Coverage
Supporting sources: ClinVar, Open Targets Platform
Multiple supporting sources are present in release evidence coverage.
- ClinVar: Variant/condition source context; not diagnostic advice, treatment guidance, or clinical decision support. NCBI public data; reuse subject to NCBI policies; citation. Source freshness: refresh recommended; assessed Jun 9, 2026; next review Jul 9, 2026. Snapshot freshness: refresh recommended; assessed Jun 9, 2026; next review Jul 9, 2026; gene_condition_source_id-2026-06-14-paper120, 12 records.
- Open Targets Platform: Source-attributed evidence signal; scores are not clinical truth or a combined confidence score. CC0 1.0; citation. Source freshness: refresh recommended; assessed Jun 9, 2026; next review Jul 9, 2026. Snapshot freshness: refresh recommended; assessed Jun 9, 2026; next review Jul 9, 2026; api-v4-graphql-2026-06-14-paper120, 120 records.
Evidence Rows evidence_rows.jsonl
| Source | Type | Statement | Open Targets score |
|---|---|---|---|
| ClinVar ClinVarGeneCondition:120892:LRRK2:C0030567:MONDO:0005180 | clinical variant context | ClinVar gene_condition_source_id reports LRRK2 in relation to Parkinson disease (MONDO:0005180) via MONDO. | not scored |
| Open Targets Platform OT:ENSG00000188906:MONDO_0005180 | target disease association | Open Targets reports LRRK2 as associated with Parkinson disease. | 0.880 |
Open Targets score breakdown
Source-attributed signals reported by Open Targets for OT:ENSG00000188906:MONDO_0005180. Each value is Open Targets' own
per-datatype or per-datasource score — not truth, clinical validity, or
a combined confidence score. Labels such as clinical and clinical_precedence are Open Targets' own datatype and
datasource names, not a clinical-use or clinical-validity signal for this
association. The overall score is Open Targets' own aggregate over these
datasources; because those datasources can overlap with evidence from
other sources, the overall score is not an independent line of
corroboration.
-
literature0.997 -
genetic_association0.927 -
genetic_literature0.869 -
affected_pathway0.555
-
europepmc0.997 -
uniprot_variants0.982 -
genomics_england0.963 -
eva0.924 -
gwas_credible_sets0.901 -
clingen0.608 -
uniprot_literature0.608 -
orphanet0.608 -
crispr_screen0.555 -
gene_burden0.152
Caveats
- Public-candidate draft; research-use only and not a clinical finding.
- AI/referee review artifacts are advisory and do not replace human scientific review.
- ClinVar gene-condition context has not passed human scientific review.
- ClinVar gene-condition context is provenance only; not diagnostic, treatment, or clinical decision-making guidance.
- Open Targets scores are source-attributed evidence signals, not truth or clinical validity scores.
- Open Targets target-disease association context is not diagnostic, treatment, or clinical decision-making guidance.
Source names identify provenance only and do not imply endorsement by HGNC, MONDO, Open Targets, ClinVar, NCBI, or any upstream source.