RS887391 Unknown gene

Other Chr 19:41479716
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What This Variant Does
"rs887391 was the most strongly associated SNP in the 19q13 region, which was a region highly associa..."
GWAS Studies (1)
Trait Risk Allele OR / Beta P-value Study
Prostate cancer (SNP x SNP interaction) OR: 1.31 2E-6 PubMed
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