Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs3844283
rs3844283
0.010 GeneticVariation BEFREE We discovered a comparatively frequent coding variant of the enigmatic human IRAK2, L392V (rs38</span>44283), which is found homozygously in ∼15% of Caucasians, to be associated with a reduced ability to induce interferon-alpha in primary human plasmacytoid dendritic cells in response to hepatitis C virus (HCV). 26250868

2015