RS34481144 Unknown gene

Other Chr 11:320836
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What This Variant Does
"SNP-mediated disruption of CTCF binding at the IFITM3 promoter is associated with risk of severe influenza in humans."
GWAS Studies (1)
Trait Risk Allele OR / Beta P-value Study
PLA2G10 protein levels T OR: 0.1 8E-83 PubMed
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