Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1800896
IL19 ; IL10
0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs2430561
IFNG ; IFNG-AS1
0.590 0.760 12 68158742 intron variant T/A snv 0.36 50
rs187238
IL18
0.602 0.680 11 112164265 intron variant C/A;G snv 48
rs1946518
IL18
0.602 0.760 11 112164735 intron variant T/G snv 0.60 46
rs755622
MIF-AS1 ; MIF
0.611 0.720 22 23894205 intron variant G/C snv 0.26 44
rs2569190
CD14 ; TMCO6
0.620 0.560 5 140633331 intron variant A/G snv 0.57 39
rs153109
IL27
0.623 0.600 16 28507775 intron variant T/C snv 0.43 37
rs12212067
FOXO3
0.716 0.320 6 108659993 intron variant T/G snv 0.14 20
rs2069837
IL6-AS1 ; IL6
0.724 0.520 7 22728408 intron variant A/C;G snv 18
rs352139
TLR9
0.732 0.320 3 52224356 intron variant T/C snv 0.51 0.54 18
rs1861494
IFNG-AS1 ; IFNG
0.716 0.400 12 68157629 intron variant C/T snv 0.75 15
rs2069718
IFNG ; IFNG-AS1
0.742 0.320 12 68156382 intron variant A/G;T snv 0.50 14
rs3117582
BAG6 ; APOM
0.716 0.440 6 31652743 intron variant T/G snv 7.1E-02 14
rs11674595
IL1R2
0.763 0.200 2 101994530 intron variant T/C snv 0.22 13
rs2243115
IL12A-AS1 ; IL12A
0.776 0.320 3 159988493 intron variant T/G snv 0.10 12
rs7453920
HLA-DQB2
0.752 0.440 6 32762235 intron variant A/G;T snv 10
rs3093662
TNF
0.851 0.200 6 31576412 intron variant A/G snv 7.1E-02 9
rs4851527
IL1R2
0.790 0.160 2 102005914 intron variant A/G snv 0.63 7
rs9420907
STN1
0.790 0.320 10 103916707 intron variant C/A;G snv 7
rs10421768
HAMP
0.807 0.120 19 35281996 intron variant A/G snv 0.21 6
rs3917225
IL1R1
0.807 0.160 2 102152842 intron variant A/G snv 0.36 6
rs5743899
TOLLIP ; LOC105376512
0.807 0.160 11 1302334 intron variant C/T snv 0.71 6