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
rs2569190
CD14 ; TMCO6
0.620 0.560 5 140633331 intron variant A/G snv 0.57 39
rs187084
TLR9
0.641 0.480 3 52227015 intron variant A/G snv 0.38 36
rs909253
LTA ; LOC100287329
0.641 0.600 6 31572536 intron variant A/G;T snv 34
rs57095329
MIR3142HG
0.677 0.480 5 160467840 intron variant A/G snv 7.8E-02 25
rs2227306
CXCL8
0.677 0.680 4 73741338 intron variant C/T snv 0.31 21
rs10865710
PPARG
0.763 0.360 3 12311699 intron variant C/G snv 0.25 13
rs5743551
TLR1
0.742 0.240 4 38806033 intron variant T/A;C snv 12
rs12508721
IL21-AS1
0.742 0.360 4 122623509 intron variant C/T snv 0.24 11
rs1143643
IL1B
0.790 0.320 2 112830725 intron variant C/T snv 0.29 10
rs11568821
LOC105373977 ; PDCD1
0.827 0.200 2 241851760 intron variant C/G;T snv 10
rs4648068
NFKB1
0.790 0.240 4 102597148 intron variant A/G snv 0.31 9
rs212388
LOC112267968 ; LOC105378083
0.827 0.240 6 159069404 intron variant C/G;T snv 8
rs2297630
CXCL12
0.827 0.160 10 44376100 intron variant G/A;T snv 0.21 6
rs842647
REL
0.827 0.400 2 60892336 intron variant G/A snv 0.62 6
rs17446614
FOXO1
0.851 0.240 13 40565740 intron variant G/A snv 0.16 5
rs4957796
FER
0.851 0.120 5 109066439 intron variant T/C snv 0.16 5
rs6586282
CBS
0.882 0.080 21 43058387 intron variant C/T snv 5
rs2721068
FOXO1
0.882 0.160 13 40565575 intron variant T/C snv 0.38 4
rs12048215
NLRP3
0.882 0.160 1 247421289 intron variant A/G snv 0.11 3
rs17036188
PPARG
0.882 0.120 3 12299426 intron variant T/C snv 4.0E-02 3
rs2839693
CXCL12
0.882 0.120 10 44379119 intron variant T/A;C snv 3
rs2972164
PPARG
0.925 0.080 3 12292917 intron variant T/C snv 0.46 3
rs4684846
PPARG
0.882 0.080 3 12297350 intron variant A/G snv 0.28 3