RS3026393 Unknown gene

Other Chr 11:31790667
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What This Variant Does
"rs3026390 and rs3026393 showed significant association with high myopia. For rs3026393, the genotype..."
GWAS Studies (1)
Trait Risk Allele OR / Beta P-value Study
Neuroticism A OR: 5.8 7E-9 PubMed
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