Table 3.
Overlap of TAGC asthma-associated SNPs with GWAS catalog association signals by disease group
| Disease Group | Number of GWAS catalog association signals |
Number of SNPs associated with asthma at Prandom≤10−4 in the multi- ancestry meta-analysis |
P-value for overlap |
|---|---|---|---|
| Cardiovascular | 743 | 20 | 7.8 × 10−42 |
| Body size and morphology | 346 | 2 | 5.0 × 10−4 |
| Immune/Autoimmune | 480 | 49 | 3.0 × 10−129 |
| Nervous system | 242 | 4 | 1.4 × 10−8 |
| Blood | 594 | 10 | 1.3 × 10−19 |
| Neuropsychiatric | 114 | 5 | 1.5 × 10−12 |
| Cancer | 417 | 7 | 4.0 × 10−14 |
| Endocrine system | 276 | 2 | 4.0 × 10−4 |
| Digestive system | 347 | 16 | 1.4 × 10−37 |
| Eyes | 177 | 2 | 2.0 × 10−4 |
| Respiratory system | 85 | 2 | 3.6 × 10−5 |
| Infectious disease/Infection | 104 | 2 | 5.3 × 10−5 |
| Urinary system | 144 | 1 | 1.5 × 10−2 |
| Alcohol, smoking, and illicit substances | 30 | 0 | 1 |
| Musculoskeletal system | 132 | 0 | 1 |
Overlap of TAGC asthma-associated SNPs with association signals of all diseases/traits in the GWAS catalog3 was investigated for all TAGC SNPs having Prandom≤10−4 in the multi-ancestry meta-analysis; diseases from the GWAS catalog were grouped according to the disease classification proposed by Wang et al.37 (note that the “Digestive system” group includes Crohn's Disease, a subtype of Inflammatory Bowel Disease). The significance of overlap was estimated by the binomial tail probability for observing the shown number of TAGC asthma SNPs among the number of SNPs reported in the GWAS catalog for a group of diseases (for example, the probability of observing 20 or more asthma SNPs with Prandom≤10−4 among the 743 cardiovascular SNPs is shown in the last column); a conservative Bonferroni adjusted significance threshold for enrichment in shared associations is 0.05/15=0.003 (for the 15 disease groups investigated).