RS7702187 Unknown gene

Other Chr 5:9332169
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What This Variant Does
"rs7702187 increases susceptibility to Parkinson's disease 1.74 times for carriers of the A allele rs..."
GWAS Studies (1)
Trait Risk Allele OR / Beta P-value Study
Parkinson's disease OR: 1.74 8E-6 PubMed
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