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. Author manuscript; available in PMC: 2017 Feb 1.
Published in final edited form as: Transl Res. 2015 May 7;168:22–39. doi: 10.1016/j.trsl.2015.04.016

Table 2.

Asthma susceptibility polymorphisms discovered through endophenotypes. The entries of the table have been ordered based on the dates in which the studies were published from the bottom to the top.

Study Endophenotype Ancestry Control + Case (Replicates included) Genes Variants Reference
European AFAM Hispanic Asian
Genome-wide association study of lung function decline in adults with and without asthma. Lung function decline 16136 DLEU7 rs9316500 23
A large-scale, consortium-based genomewide association study of asthma. IgE levels 30478 IL18R1, HLA-DQ, IL33, SMAD3, GSDMB, GSDMA, IL2RB, HLA-DRB1, FCER1A, IL13, STAT6, IL4-R/IL21R rs3771166, rs9273349, rs1342326, rs744910, rs2305480, rs3894194, rs2284033, rs9271300, rs2252226, rs20541, rs167769, rs1859308 10
Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction. Eosinophil counts 26722 IL1RL1, IKZF2, GATA2, IL5, SH2B3 rs1420101, rs12619285, rs4143832, rs9494145, rs3184504 21
Effect of variation in CHI3L1 on serum YKL-40 level, risk of asthma, and lung function. YKL-40 levels 1772 CHI3L1 rs4950928 22