Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs72928038
BACH2
0.695 0.360 6 90267049 intron variant G/A snv 0.11 19
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 16
rs706778
IL2RA
0.695 0.320 10 6056986 intron variant C/T snv 0.46 15
rs7731626
ANKRD55
0.716 0.240 5 56148856 intron variant G/A snv 0.30 15
rs10174238
STAT4
0.724 0.200 2 191108308 intron variant G/A snv 0.70 12
rs4409785 0.752 0.240 11 95578258 intron variant T/C snv 0.13 12
rs2187668
LOC107986589 ; HLA-DQA2 ; HLA-DQA1
0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03 11
rs1800469
B9D2 ; TGFB1
0.547 0.760 19 41354391 intron variant A/G snv 0.69 10
rs3830041
NOTCH4
0.752 0.280 6 32223562 intron variant C/T snv 0.11 9
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 9
rs11221332
ETS1
0.763 0.280 11 128511079 intron variant C/A;T snv 8
rs6651252
LINC00824
0.790 0.200 8 128554935 intron variant T/C snv 0.19 8
rs11066301
PTPN11
0.827 0.200 12 112433568 intron variant A/G snv 0.30 7
rs1480380
HLA-DMB
0.763 0.360 6 32945469 intron variant C/T snv 0.11 7
rs2104286
IL2RA
0.662 0.440 10 6057082 intron variant T/C snv 0.18 7
rs2855812
MICB
0.790 0.360 6 31504943 intron variant G/T snv 0.23 7
rs71508903
ARID5B
0.807 0.160 10 62020112 intron variant C/T snv 0.15 7
rs71624119
ANKRD55
0.776 0.200 5 56144903 intron variant G/A snv 0.17 7
rs13101828
DGKQ
0.851 0.160 4 971932 intron variant A/G snv 0.43 6
rs1378942
CSK
0.790 0.240 15 74785026 intron variant C/A;T snv 6
rs2451258
LOC112267968
0.807 0.160 6 159085568 intron variant C/T snv 0.75 6
rs2812378
CCL21
0.790 0.200 9 34710263 intron variant G/A;C snv 6
rs10774624
LINC02356
0.882 0.160 12 111395984 intron variant G/A snv 0.67 5
rs12531711
TNPO3
0.827 0.200 7 128977412 intron variant A/C;G snv 5
rs2431098 0.827 0.240 5 160460329 intron variant A/G;T snv 5