RS34637584 LRRK2
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What This Variant Does
"First discovered in 2004, rs34637584 is a SNP indicating a position within the LRRK2 that encodes a ...
Associated Conditions
Autosomal dominant Parkinson disease 8
Inborn genetic diseases
Young-onset Parkinson disease
Parkinson disease
late-onset
LRRK2-related disorder
Autosomal dominant Parkinson disease 8
Inborn genetic diseases
Young-onset Parkinson disease
Parkinson disease
late-onset
LRRK2-related disorder
GWAS Studies (6)
| Trait | Risk Allele | OR / Beta | P-value | Study |
|---|---|---|---|---|
| Parkinson's disease or first degree relation to individual with Parkinson's disease | A | OR: 2.43 | 4E-148 | PubMed |
| Parkinson's disease | A | OR: 9.62 | 2E-28 | PubMed |
| Parkinson's disease | G | OR: 1.59 | 7E-17 | PubMed |
| Parkinson's disease | G | OR: 1.81 | 3E-12 | PubMed |
| Parkinson's disease | A | OR: 2.27 | 7E-12 | PubMed |
| Parkinson's disease | G | OR: 1.64 | 2E-11 | PubMed |
Other Variants in LRRK2