Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13098911
CCR3
0.882 0.200 3 46193709 intron variant C/G;T snv 5
rs17035378
PLEK ; LOC101927723
0.882 0.200 2 68371823 intron variant T/A;C snv 5
rs2816316
LOC105371664
0.882 0.200 1 192567683 intron variant C/A snv 0.79 5
rs296547
MROH3P
0.882 0.200 1 200923009 intron variant T/C snv 0.53 5
rs4675374
ICOS ; LOC101927840
0.882 0.200 2 203937855 intron variant T/C snv 0.65 5
rs947474
LINC02649 ; LINC02656
0.827 0.440 10 6348488 intron variant G/A snv 0.79 5
rs9979383
RUNX1
0.925 0.200 21 35343463 intron variant C/G;T snv 5
rs10892258
LOC105369519
0.925 0.120 11 118709156 intron variant G/A snv 0.19 4
rs2074404
LRRC37A2 ; WNT3
0.925 0.120 17 46788073 intron variant T/G snv 0.27 4
rs2305767
MYO9B
0.882 0.280 19 17183487 intron variant C/T snv 0.70 4
rs864537
CD247
0.925 0.200 1 167442147 intron variant A/G snv 0.29 4
rs9286879 0.851 0.200 1 172893094 intron variant A/G snv 0.32 4
rs13015714
IL18R1
0.882 0.200 2 102355405 intron variant G/T snv 0.77 3
rs2069772
IL2
0.925 0.200 4 122451978 intron variant T/A;C snv 3
rs212402
LOC105378083
1.000 0.080 6 159051263 intron variant G/A snv 0.66 3
rs2474619
BACH2
0.882 0.360 6 90170316 intron variant C/A snv 0.72 3
rs55743914
PTPRK
0.882 0.160 6 127972417 intron variant C/T snv 0.18 3
rs6432714
IFIH1
0.882 0.160 2 162280842 intron variant A/T snv 0.16 3
rs654690
LOC112267968
1.000 0.080 6 159093746 intron variant T/A;C snv 3
rs76830965
IL12A-AS1
0.925 0.120 3 159919889 intron variant C/A;G;T snv 3
rs10188217
PUS10
0.925 0.080 2 60990407 intron variant T/A;C snv 2
rs10203477
LINC01185
0.925 0.200 2 60877850 intron variant A/T snv 0.48 2
rs11123810
AFF3
0.925 0.200 2 100142823 intron variant T/C snv 0.37 2
rs12734338
PPP1R12B
0.925 0.120 1 202500595 intron variant T/C snv 2
rs1353248
IL12A-AS1
0.925 0.120 3 159905770 intron variant C/T snv 0.32 2