rs2251086
This is a intron variant variant in the LOC107984782 gene.
▶GWAS Catalog Trait Associations (1)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
GWAS Catalog Trait Associations (1)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
Parkinson disease
Kim JJ et al. “Multi-ancestry genome-wide association meta-analysis of Parkinson's disease.” Nature Genetics 56(1):27-36 (2024)
Allele T
OR —
p 5.0e-22
N 2,525,730
Meta-analysisLarge GWAS
multi-ancestry
Nalls MA et al. “Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies.” The Lancet. Neurology 18(12):1091-1102 (2019)
Allele T
OR 0.12
p 6.0e-18
N 482,730
Meta-analysisLarge GWAS
European
Pan H et al. “Genome-wide association study using whole-genome sequencing identifies risk loci for Parkinson's disease in Chinese population.” Npj Parkinson's Disease 9(1):22 (2023)
Allele T
OR 0.16
p 1.0e-9
N 4,450
Large GWAS
East Asian
This variant is in our database but has no known associations or PRS memberships yet.
Gene information from NCBI Gene. Variant classifications from ClinVar.
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