Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7216389
GSDMB
0.732 0.440 17 39913696 intron variant C/T snv 0.60 14
rs767455
TNFRSF1A
0.742 0.400 12 6341779 synonymous variant T/C snv 0.37 0.40 13
rs10488631
TNPO3
0.742 0.280 7 128954129 upstream gene variant T/C snv 9.0E-02 13
rs2304256
TYK2
0.732 0.360 19 10364976 missense variant C/A snv 0.27 0.23 13
rs11065979 0.851 0.200 12 111621753 intergenic variant C/T snv 0.30 12
rs2872507 0.752 0.360 17 39884510 intergenic variant G/A;T snv 12
rs8067378 0.752 0.240 17 39895095 regulatory region variant A/G snv 0.50 12
rs11889341
STAT4
0.732 0.480 2 191079016 intron variant C/T snv 0.21 12
rs6478109
TNFSF15
0.752 0.320 9 114806486 upstream gene variant A/G snv 0.74 12
rs3824260
CYP7A1
0.742 0.160 8 58500631 upstream gene variant A/G;T snv 11
rs2305480
GSDMB
0.763 0.280 17 39905943 missense variant G/A snv 0.40 0.35 10
rs6478108
TNFSF15
0.763 0.200 9 114796423 intron variant C/T snv 0.73 10
rs2290400
GSDMB
0.790 0.360 17 39909987 intron variant T/C snv 0.48 9
rs9303277
IKZF3
0.790 0.240 17 39820216 intron variant C/T snv 0.52 9
rs694739
LOC102723878
0.763 0.320 11 64329761 upstream gene variant A/G snv 0.28 9
rs12373124
SPPL2C ; MAPT-AS1
0.790 0.120 17 45846853 synonymous variant T/C snv 0.15 0.14 9
rs10181656
STAT4
0.763 0.360 2 191105153 intron variant G/C snv 0.79 9
rs1800693
TNFRSF1A
0.776 0.360 12 6330843 non coding transcript exon variant T/C snv 0.36; 4.0E-06 0.38 9
rs2205960
TNFSF4
0.763 0.400 1 173222336 intergenic variant G/A;T snv 9
rs3135363 0.776 0.360 6 32421871 intergenic variant A/G snv 0.24 8
rs3807306
IRF5
0.776 0.320 7 128940626 intron variant G/A;T snv 8
rs10168266
STAT4
0.776 0.400 2 191071078 intron variant C/T snv 0.19 8
rs7775055 0.790 0.200 6 32690139 TF binding site variant T/C snv 6.2E-02 7
rs12708716
CLEC16A
0.807 0.320 16 11086016 intron variant A/G snv 0.37 7
rs393152
LINC02210 ; LINC02210-CRHR1
0.851 0.160 17 45641777 non coding transcript exon variant A/G snv 0.18 0.29 7