RS16872571 Unknown gene

Other Chr 4:10725229
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What This Variant Does
"[GWAS:None]"
GWAS Studies (2)
Trait Risk Allele OR / Beta P-value Study
Myopia (pathological) — — 2E-10 PubMed
Vitiligo C OR: 1.21 2E-8 PubMed
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