Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs310746 1.000 0.040 3 12218116 intergenic variant C/T snv 0.93 1
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs10744676
KCNA5
0.925 0.080 12 5043783 upstream gene variant C/T snv 0.88 2
rs6659932
IL12RB2
0.827 0.240 1 67336688 intron variant A/C snv 0.81 5
rs344781
PLAUR
0.807 0.200 19 43670636 upstream gene variant C/T snv 0.80 7
rs1883832
CD40
0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80 52
rs661968
AVEN ; CHRM5
1.000 0.040 15 33968868 5 prime UTR variant C/T snv 0.80 1
rs1857066
LOC100506023 ; TNFSF4
1.000 0.040 1 173363490 non coding transcript exon variant A/C snv 0.79 1
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs1005714
NUP85 ; GGA3
1.000 0.040 17 75228544 5 prime UTR variant G/C snv 0.78 1
rs959173
CAV1
0.925 0.120 7 116542000 intron variant C/T snv 0.78 2
rs2904880
CD19 ; RABEP2
1.000 0.040 16 28933075 missense variant C/G snv 0.72 0.76 5
rs802791
ATG5
0.851 0.160 6 106121395 intron variant T/C snv 0.75 4
rs1521 0.882 0.320 6 31382927 upstream gene variant C/T snv 0.74 3
rs230534
NFKB1
0.882 0.120 4 102527884 intron variant T/C snv 0.73 3
rs25487
XRCC1
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs7172677 0.925 0.080 15 75132252 intergenic variant A/C snv 0.71 2
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs2910164
MIR3142HG ; MIR146A
0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs10174238
STAT4
0.724 0.200 2 191108308 intron variant G/A snv 0.70 14
rs2844494 0.925 0.160 6 31515638 upstream gene variant C/A snv 0.70 2
rs2516398 0.882 0.200 6 31513749 upstream gene variant G/T snv 0.70 3
rs4134466
ATG5
1.000 0.040 6 106129493 intron variant A/G snv 0.70 1
rs4939364
MS4A1
1.000 0.040 11 60464852 intron variant A/G snv 0.66 1
rs4076852
PXK
1.000 0.040 3 58389559 intron variant G/A snv 0.65 1