Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2104286
IL2RA
0.662 0.440 10 6057082 intron variant T/C snv 0.18 25
rs72928038
BACH2
0.695 0.360 6 90267049 intron variant G/A snv 0.11 19
rs7517847
IL23R ; C1orf141
0.689 0.600 1 67215986 intron variant T/G snv 0.37 19
rs4676410
GPR35
0.716 0.240 2 240624322 intron variant G/A snv 0.26 17
rs11221332
ETS1
0.763 0.280 11 128511079 intron variant C/A;T snv 13
rs4129267
IL6R
0.807 0.200 1 154453788 intron variant C/G;T snv 13
rs17293632
SMAD3
0.763 0.240 15 67150258 intron variant C/T snv 0.17 12
rs2301436
FGFR1OP
0.752 0.320 6 167024500 intron variant C/T snv 0.42 11
rs4845604
RORC
0.776 0.200 1 151829204 intron variant G/A;C;T snv 10
rs11168249
HDAC7
0.807 0.120 12 47814585 intron variant T/C snv 0.50 9
rs2284553
IFNGR2
0.776 0.240 21 33404389 intron variant A/G snv 0.69 9
rs26528
IL27
0.807 0.200 16 28506388 intron variant T/C snv 0.43 9
rs3024493
IL19 ; IL10
0.776 0.280 1 206770623 intron variant C/A;T snv 0.11 9
rs3774937
NFKB1
0.776 0.280 4 102513096 intron variant T/C snv 0.26 9
rs61839660
IL2RA
0.776 0.280 10 6052734 intron variant C/T snv 5.7E-02 9
rs1182188
GNA12
0.827 0.120 7 2830351 intron variant T/C snv 0.26 8
rs17622378
IRF1-AS1
0.790 0.200 5 132442760 intron variant A/G snv 0.28 8
rs2812378
CCL21
0.790 0.200 9 34710263 intron variant G/A;C snv 8
rs582757
TNFAIP3
0.776 0.320 6 137876687 intron variant C/T snv 0.70 8
rs6651252
LINC00824
0.790 0.200 8 128554935 intron variant T/C snv 0.19 8
rs71624119
ANKRD55
0.776 0.200 5 56144903 intron variant G/A snv 0.17 8
rs11229555
GLYAT
0.827 0.120 11 58641214 intron variant G/T snv 0.21 7
rs12942547
STAT3
0.807 0.200 17 42375526 intron variant A/G;T snv 7
rs1847472
BACH2
0.807 0.200 6 90263440 intron variant C/A snv 0.25 7
rs1860545
TNFRSF1A
0.790 0.200 12 6337611 intron variant G/A snv 0.31 7