Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800896
IL19 ; IL10
0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs7975232
VDR
0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 56
rs2430561
IFNG ; IFNG-AS1
0.590 0.760 12 68158742 intron variant T/A snv 0.36 50
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 41
rs5743836
TLR9
0.658 0.440 3 52226766 intron variant A/G snv 0.20 31
rs1535
FADS2
0.752 0.240 11 61830500 intron variant A/G snv 0.31 24
rs744166
STAT3
0.689 0.560 17 42362183 intron variant A/G snv 0.48 22
rs2187668
LOC107986589 ; HLA-DQA2 ; HLA-DQA1
0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03 20
rs4696480
TLR2
0.716 0.400 4 153685974 intron variant T/A snv 0.45 19
rs7517847
IL23R ; C1orf141
0.689 0.600 1 67215986 intron variant T/G snv 0.37 19
rs2071746
HMOX1
0.708 0.320 22 35380679 intron variant A/T snv 0.49 18
rs352139
TLR9
0.732 0.320 3 52224356 intron variant T/C snv 0.51 0.54 18
rs4676410
GPR35
0.716 0.240 2 240624322 intron variant G/A snv 0.26 17
rs1861494
IFNG-AS1 ; IFNG
0.716 0.400 12 68157629 intron variant C/T snv 0.75 15
rs1893217
PTPN2
0.742 0.440 18 12809341 intron variant A/G snv 0.12 14
rs3789243
ABCB1
0.776 0.120 7 87591570 intron variant A/G snv 0.50 14
rs6887695 0.732 0.440 5 159395637 intron variant G/C snv 0.35 14
rs6920220 0.742 0.440 6 137685367 intron variant G/A snv 0.16 14
rs11221332
ETS1
0.763 0.280 11 128511079 intron variant C/A;T snv 13
rs17293632
SMAD3
0.763 0.240 15 67150258 intron variant C/T snv 0.17 12
rs4845604
RORC
0.776 0.200 1 151829204 intron variant G/A;C;T snv 10
rs516246
FUT2 ; LOC105447645
0.925 0.160 19 48702915 intron variant C/T snv 0.38 0.45 10
rs6478108
TNFSF15
0.763 0.200 9 114796423 intron variant C/T snv 0.73 10
rs7495132
CRTC3 ; CRTC3-AS1
0.790 0.080 15 90629669 intron variant C/T snv 0.12 10