Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7820268
IDO1
0.925 0.080 8 39920010 intron variant C/T snv 0.28 2
rs7774954
HLA-DQB2
0.925 0.120 6 32756412 3 prime UTR variant C/A;T snv 5.9E-02 2
rs7764491
HLA-DPA2
1.000 0.040 6 33093063 non coding transcript exon variant C/G snv 5.4E-02 1
rs7763822
HLA-DPA2
1.000 0.040 6 33092651 intron variant C/T snv 5.4E-02 1
rs77583790
IL12A-AS1
0.882 0.080 3 159976265 intron variant G/A;C snv 3
rs774359492
WDHD1
0.807 0.200 14 55008684 missense variant C/T snv 4.0E-06 7.0E-06 7
rs7665090
MANBA
0.807 0.280 4 102630446 downstream gene variant A/G snv 0.55 6
rs763361
CD226
0.689 0.520 18 69864406 missense variant T/A;C snv 4.0E-06; 0.52 21
rs76246107
PRR12
0.851 0.160 19 49618017 intron variant G/A snv 7.7E-02 4
rs7601754
STAT4
0.882 0.160 2 191075725 intron variant G/A;T snv 3
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs7574685
LINC01173
0.925 0.040 2 234702877 intron variant T/C snv 0.59 2
rs755622
MIF-AS1 ; MIF
0.611 0.720 22 23894205 intron variant G/C snv 0.26 44
rs755460305
KNG1
0.882 0.080 3 186732650 missense variant C/A snv 4
rs753727908
FCGR3A
1.000 0.040 1 161544759 missense variant C/G;T snv 4.0E-06; 8.0E-06 1
rs744600 0.851 0.160 2 190700031 intron variant G/T snv 0.60 4
rs7190018
ITGAM
1.000 0.040 16 31290157 intron variant G/A;C snv 1
rs7172677 0.925 0.080 15 75132252 intergenic variant A/C snv 0.71 2
rs7130875 1.000 0.040 11 118742965 intron variant T/C snv 0.22 1
rs7126354
MS4A1
1.000 0.040 11 60463593 intron variant C/T snv 0.64 1
rs707939
MSH5-SAPCD1 ; MSH5
0.851 0.200 6 31758911 intron variant C/A snv 0.34 0.26 5
rs704840
LOC100506023 ; TNFSF4
0.851 0.240 1 173257056 intergenic variant T/G snv 0.29 4
rs7044343
LOC107987046 ; IL33
0.752 0.520 9 6254208 intron variant C/T snv 0.51 13
rs702966
PHRF1
0.925 0.080 11 611919 3 prime UTR variant C/G snv 0.33 2
rs6941112
CYP21A2 ; STK19
0.882 0.120 6 31978837 intron variant G/A snv 0.25 3