Source: GWASDB ×
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs2476601
rs2476601
PTPN22 ; AP4B1-AS1
13 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 0.700 1.000 1 2011 2011
dbSNP: rs653178
rs653178
ATXN2
17 0.672 0.600 12 111569952 intron variant C/T snv 0.67 0.700 1.000 1 2011 2011
dbSNP: rs744166
rs744166
STAT3
3 0.689 0.560 17 42362183 intron variant A/G snv 0.48 0.700 1.000 1 2011 2011
dbSNP: rs3093059
rs3093059
CRP
2 0.752 0.520 1 159715346 upstream gene variant A/G snv 0.13 0.700 1.000 1 2011 2011
dbSNP: rs2187668
rs2187668
HLA-DQA1 ; HLA-DQA2 ; LOC107986589
10 0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03 0.700 1.000 1 2011 2011
dbSNP: rs2542151
rs2542151 		6 0.763 0.480 18 12779948 upstream gene variant G/T snv 0.83 0.700 1.000 1 2011 2011
dbSNP: rs917997
rs917997 		6 0.701 0.480 2 102454108 downstream gene variant T/A;C snv 0.700 1.000 1 2011 2011
dbSNP: rs7216389
rs7216389
GSDMB
3 0.732 0.440 17 39913696 intron variant C/T snv 0.60 0.900 0.889 4 2007 2018
dbSNP: rs17810546
rs17810546
IL12A-AS1
6 0.827 0.440 3 159947262 intron variant A/G snv 8.2E-02 0.700 1.000 1 2011 2011
dbSNP: rs1893217
rs1893217
PTPN2
8 0.742 0.440 18 12809341 intron variant A/G snv 0.12 0.700 1.000 1 2011 2011
dbSNP: rs9268853
rs9268853
HLA-DRB9
8 0.790 0.440 6 32461866 intron variant T/C snv 0.29 0.700 1.000 1 2012 2012
dbSNP: rs2066847
rs2066847
NOD2
2 0.716 0.400 16 50729868 frameshift variant C/-;CC delins 1.5E-02 0.700 1.000 1 2011 2011
dbSNP: rs4505848
rs4505848
KIAA1109
2 0.776 0.400 4 122211337 intron variant A/G snv 0.29 0.700 1.000 1 2011 2011
dbSNP: rs1342326
rs1342326 		2 0.790 0.360 9 6190076 intergenic variant A/C snv 0.21 0.840 1.000 3 2010 2020
dbSNP: rs2872507
rs2872507 		7 0.752 0.360 17 39884510 intergenic variant G/A;T snv 0.720 1.000 3 2010 2012
dbSNP: rs2290400
rs2290400
GSDMB
6 0.790 0.360 17 39909987 intron variant T/C snv 0.48 0.820 1.000 2 2010 2016
dbSNP: rs1058808
rs1058808
ERBB2
1 0.658 0.360 17 39727784 missense variant C/G snv 0.61 0.52 0.710 1.000 1 2011 2013
dbSNP: rs12232497
rs12232497 		3 0.701 0.360 17 39883866 intergenic variant T/C snv 0.35 0.700 1.000 1 2011 2011
dbSNP: rs3939286
rs3939286 		2 0.776 0.360 9 6210099 regulatory region variant T/A;C snv 0.710 1.000 1 2010 2020
dbSNP: rs762421
rs762421
GATD3A
3 0.851 0.360 21 44195678 intron variant G/A snv 0.700 1.000 1 2011 2011
dbSNP: rs7775228
rs7775228 		5 0.790 0.360 6 32690302 TF binding site variant T/C snv 0.15 0.810 0.500 1 2011 2020
dbSNP: rs11465804
rs11465804
IL23R
3 0.752 0.320 1 67236843 intron variant T/G snv 4.4E-02 5.4E-02 0.700 1.000 1 2011 2011
dbSNP: rs1738074
rs1738074
TAGAP ; LOC105378083 ; LOC107986664
5 0.790 0.320 6 159044945 5 prime UTR variant T/C snv 0.49 0.700 1.000 1 2011 2011
dbSNP: rs2301436
rs2301436
FGFR1OP
4 0.752 0.320 6 167024500 intron variant C/T snv 0.42 0.700 1.000 1 2011 2011
dbSNP: rs2327832
rs2327832 		6 0.790 0.320 6 137651931 intergenic variant A/G snv 0.16 0.700 1.000 1 2011 2011