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Gene

LRRK2

LRRK2 is a gene. This site has 26 published variants inside it and 1 near it, each from a published genetic study, joining it to 7 condition pages.

Conditions it is linked to

• Blood Cell Counts
• Celiac Disease
• Cholesterol (LDL, HDL and Total)
• Height
• Hemorrhage from Gastrointestinal Ulcer
• Parkinson's Disease
• Ulcerative Colitis

Variants inside LRRK2 (26)

• rs33939927 · Autosomal dominant Parkinson disease 8
• rs34015634 · Autosomal dominant Parkinson disease 8
• rs34805604 · Autosomal dominant Parkinson disease 8
• rs34995376 · Autosomal dominant Parkinson disease 8
• rs35801418 · Autosomal dominant Parkinson disease 8
• rs35870237 · Autosomal dominant Parkinson disease 8
• rs142436514 · CNTN1 protein levels
• rs10506148 · Height
• rs552964187 · Hemorrhage from gastrointestinal ulcer (PheCode 531.1)
• rs2499873877 · Interstitial pulmonary disease
• rs2723261 · Mean platelet volume
• rs2638272 · mean platelet volume (MPV, maximum, inv-norm transformed)
• rs2404581 · mean platelet volume (MPV, minimum, inv-norm transformed)
• rs10878220 · Mean platelet volume during first trimester of pregnancy
• rs1491942 · Parkinson's disease
• rs17443414 · Parkinson's disease
• rs190807041 · Parkinson's disease
• rs34594498 · Parkinson's disease
• rs34637584 · Parkinson's disease
• rs76904798 · Parkinson's disease
• rs117073808 · Parkinson's disease or first degree relation to individual with Parkinson's disease
• rs17466626 · Pediatric autoimmune diseases
• rs529898481 · Platelet count
• rs538387289 · Platelet distribution width
• rs1491934 · Putamen iron levels (R2* MRI)
• rs1907631 · Total cholesterol levels

Variants near LRRK2 (1)

Positions outside the gene, filed under it because it is the closest. A variant near a gene does not always act through it.

• rs17442910 · Platelet count

See LRRK2 with everything it connects to on the Gene Knowledge Graph, or as data at /api/v1/genes/LRRK2.

A gene page gathers published research; it is not a test result and not medical advice. If a gene matters to your health, talk to a doctor or a genetic counsellor.