Table 1.
Chr | SNP ID | Risk allele | Mapped genes | COVID-19 patients (n = 475) vs. controls (n = 2217) |
Hospitalized COVID-19 patients (n = 146) vs. controls (n = 2217) | |||||
---|---|---|---|---|---|---|---|---|---|---|
P/Padj | AF (case/ctrl) | OR (95% CI) | P/Padj | AF (case/ctrl) | OR(95% CI) | GWAS catalog OR (95% CI) |
||||
3 | rs71325088 | C | SLC6A20, LZTFL1 | 0.0007/0.007 | 0.13/0.09 | 1.46 (1.17–1.81) | 0.00001/0.0001 | 0.16/0.09 | 2.10 (1.50–2.92) | 1.9a (1.73–2.0) |
3 | rs11385942 | A | LZTFL1 | 0.0005/0.005 | 0.13/0.09 | 1.47 (1.18–1.82) | 0.000006/0.00006 | 0.16/0.09 | 2.14 (1.54–2.99) | 2.11b (1.70–2.61) |
3 | rs73064425 | T | AC099782.3, LZTFL1 | 0.0008/0.007 | 0.13/0.09 | 1.45 (1.17–1.80) | 0.00001/0.00009 | 0.16/0.09 | 2.13 (1.52–2.97) | 1.7a NR |
6 | rs143334143 | A | CCHCR1 | 0.7/1 | 0.09/0.09 | 0.94 (0.73–1.22) | 0.4/1 | 0.10/0.09 | 1.18 (0.78–1.80) | 1.3a (1.27–1.48) |
9 | rs657152 | A | ABO | 0.1/0.891 | 0.47/0.44 | 1.13 (0.98–1.31) | 0.1/1 | 0.48/0.44 | 1.22 (0.95–1.55) | 1.32b (1.20–1.47) |
12 | rs6489867 | C | OAS1, AC004551.1 | 0.9/1 | 0.30/0.31 | 0.99 (0.85–1.16) | 0.7/1 | 0.29/0.31 | 0.96 (0.73–1.25) | 1.2a (1.14–1.25) |
19 | rs2109069 | A | DPP9 | 0.01/0.115 | 0.30/0.27 | 1.22 (1.04–1.44) | 0.1/1 | 0.30/0.27 | 1.22 (0.94–1.59) | 1.2a (1.19–1.31) |
19 | rs11085727 | T | TYK2 | 0.03/0.235 | 0.31/0.28 | 1.20 (1.02–1.40) | 0.1/1 | 0.32/0.28 | 1.23 (0.95–1.60) | 1.2a (1.18–1.31) |
21 | rs13050728 | T | AP000295.1, IFNAR2 | 0.6/1 | 0.39/0.38 | 1.04 (0.90–1.21) | 0.06/1 | 0.43/0.38 | 1.28 (0.99–1.64) | 1.2a (1.16–1.28) |
Bold represents the significant P-values after Bonferroni correction
aFrom Pairo-Castineira et al. 2021
bFrom The Severe COVID-19 GWAS Group 2020.
Bold represent the significant P-values. Chr, Chromosome number; SNP, Single nucleotide polymorphism; AF, Allele frequency; Padj, Bonferroni adjusted P-value; ctrl, controls; OR, Odds ratio; CI, Confidence interval; NR, not recorded