RS10034228 Unknown gene

Other Chr 4:111690594
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What This Variant Does
"rs10034228 is a SNP that has been associated with pathological myopia (nearsightedness) in Han Chine..."
GWAS Studies (1)
Trait Risk Allele OR / Beta P-value Study
Myopia (pathological) OR: 1.23 8E-13 PubMed
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