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. 2022 Jul 15;31(23):3945–3966. doi: 10.1093/hmg/ddac158

Table 2.

Candidate variants from the main and subtype analysis

snpid rsid A1 A2 FRQ OR OR_95L OR_95U PPR P gene
Main analysis chr3:45848457:C:T rs35731912 T C 0.09 1.784 1.723 1.847 1.000 2.32E−21 LZTFL1
chr19:10351837:C:T rs11085725 T C 0.273 1.269 1.254 1.283 1.000 1.02E−10 TYK2
chr9:133261703:A:G rs687289 A G 0.358 1.240 1.219 1.262 1.000 4.49E−10 ABO
chr19:4717660:A:G rs12610495 G A 0.27 1.216 1.188 1.244 0.990 9.91E−08 DPP9
chr9:14754866:A:G rs7023573 A G 0.285 1.207 1.185 1.231 0.954 5.21E−07 FREM1
chr17:45933112:G:A rs8065800 G A 0.328 1.194 1.145 1.247 0.925 8.90E−07 MAPT
chr4:30946048:T:C rs12512667 C T 0.444 0.850 0.828 0.873 0.922 8.95E−07 PCDH7
Subtype analysis chr19:10351837:C:T rs11085725 T C 0.272 1.309 1.294 1.325 0.999 3.24E−09 TYK2
chr19:4717660:A:G rs12610495 G A 0.267 1.286 1.257 1.316 0.993 2.87E−08 DPP9
chr13:55031860:T:C rs111671068 C T 0.012 2.802 2.794 2.810 0.806 1.43E−07 OLFM4
chr9:133271182:T:C rs550057 T C 0.266 1.262 1.238 1.286 0.939 4.56E−07 ABO
chr18:7897309:A:C rs17565758 C A 0.078 1.510 1.470 1.550 0.938 4.84E−07 PTPRM
chr21:33247902:C:T rs2834161 C T 0.371 1.250 1.175 1.331 0.923 6.10E−07 IFNAR2

We show only variants that have a PPR > 0.8 in the MAMBA analysis. A more detailed overview of all variants is shown in Supplementary Material, Table S3. snpid: id of the marker as chr:pos:alleles, genome build hg38; A1: minor allele from TopMed imputation; A2: major allele from TopMed imputation; OR/OR_95L/OR_95U: OR and 95% CI of A1; PPR: posterior probability of replication; P: P value of association.