Table 1.
Study | Number of Cases | Number of Controls | Tested polymorphisms | Significant non-MHC loci (novel) |
---|---|---|---|---|
IMSGC (2007) [42] | 931 | 1862 | 334923 | 2 |
WTCCC1 (2007) [84] | 975 | 1466 | 12374 | 0 |
Comabella (2008) [85] | 242 | 242 | 528867 | 0 |
Aulchenko (2008) [86] | 45 | 195 | 250000 | 1* |
Baranzini (2009) [87] | 978 | 883 | 551642 | 0 |
De Jager¶ (2009) [88] | 860 | 1720 | 709690 | 3* |
ANZgene (2009) [89] | 1618 | 3413 | 302098 | 2 |
Sanna (2010) [90] | 882 | 872 | 555335 | 1* |
Nischwitz (2010) [91] | 590 | 825 | 300000 | 3 |
Jakkula (2010) [92] | 68 | 136 | 297343 | 1* |
IMSGC and WTCCC2 (2011) [33] | 9772 | 17376 | 475806 | 29* |
Patsopoulos¶ (2011) [93] | 1453 | 2176 | 906600 | 3* |
Matesanz¶ (2012) [94] | 296 | 801 | 130903 | 0 |
Martinelli-Boneschi (2012) [95] | 197 | 234 | 277866 | 0 |
Case and control numbers refer to discovery datasets.
Studies that applied the conventional genome-wide significant threshold (P< 5×10−8); for the others, an arbitrary threshold (P≤10−7) was used to identify the significant loci.
Studies based on meta-analysis.