RS2107614 Unknown gene

Other Chr 12:793913
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What This Variant Does
"Potential relationship between single nucleotide polymorphisms used in forensic genetics and diseases or other traits in European population"
GWAS Studies (1)
Trait Risk Allele OR / Beta P-value Study
monocyte (fraction, mean, inv-norm transformed) T β: 0.027 1E-13 PubMed
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