Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs2234693
ESR1
0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
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
rs2569190
CD14 ; TMCO6
0.620 0.560 5 140633331 intron variant A/G snv 0.57 39
rs7216389
GSDMB
0.732 0.440 17 39913696 intron variant C/T snv 0.60 14
rs11889341
STAT4
0.732 0.480 2 191079016 intron variant C/T snv 0.21 12
rs6478108
TNFSF15
0.763 0.200 9 114796423 intron variant C/T snv 0.73 10
rs10181656
STAT4
0.763 0.360 2 191105153 intron variant G/C snv 0.79 9
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
rs10168266
STAT4
0.776 0.400 2 191071078 intron variant C/T snv 0.19 8
rs3807306
IRF5
0.776 0.320 7 128940626 intron variant G/A;T snv 8
rs12708716
CLEC16A
0.807 0.320 16 11086016 intron variant A/G snv 0.37 7
rs1860545
TNFRSF1A
0.790 0.200 12 6337611 intron variant G/A snv 0.31 7
rs4979462
TNFSF15
0.790 0.240 9 114804733 intron variant C/T snv 0.13 7
rs8070723
MAPT
0.851 0.240 17 46003698 intron variant A/G snv 0.18 7
rs919462
MAPT
0.807 0.120 17 45988374 intron variant C/T snv 0.15 7
rs1234313
TNFSF4
0.807 0.400 1 173197108 intron variant A/G snv 0.72 6
rs1256030
ESR2
0.827 0.240 14 64280452 intron variant A/G;T snv 6
rs16841904
DENND1B
0.807 0.160 1 197732862 intron variant C/T snv 0.18 6
rs1864325
MAPT
0.882 0.160 17 45900461 intron variant C/T snv 0.14 6
rs35736272
ZPBP2
0.807 0.160 17 39876427 intron variant T/C snv 0.35 6
rs3784099
RAD51B
0.807 0.320 14 68283210 intron variant G/A snv 0.43 6
rs3807307
IRF5
0.827 0.120 7 128939148 intron variant T/C snv 0.41 6