Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3212227
IL12B
0.566 0.840 5 159315942 3 prime UTR variant T/G snv 0.26 65
rs1799964
LTA ; LOC100287329 ; TNF
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19 47
rs1799724
LTA ; TNF
0.600 0.680 6 31574705 upstream gene variant C/T snv 8.5E-02 47
rs1884444
IL23R ; C1orf141
0.637 0.600 1 67168129 missense variant G/T snv 0.52 0.51 34
rs3745274
CYP2B6
0.672 0.480 19 41006936 missense variant G/A;T snv 4.0E-06; 0.27 30
rs12075
CADM3-AS1 ; ACKR1
0.724 0.240 1 159205564 missense variant G/A snv 0.51 0.66 22
rs8177374
TIRAP
0.672 0.520 11 126292948 missense variant C/T snv 0.12 0.11 22
rs12212067
FOXO3
0.716 0.320 6 108659993 intron variant T/G snv 0.14 20
rs867186
PROCR ; MMP24-AS1-EDEM2
0.752 0.120 20 35176751 missense variant A/G snv 0.10 9.7E-02 15
rs7530511
IL23R ; C1orf141
0.742 0.400 1 67219704 missense variant T/A;C snv 0.88 12
rs17860508
LOC285626
0.752 0.360 5 159333192 intron variant TTAGAG/GC delins 11
rs76980269
NOS1
0.763 0.280 12 117330794 synonymous variant G/A snv 2.8E-05 4.2E-05 10
rs5030868
G6PD
0.827 0.160 X 154534419 missense variant G/A snv 2.6E-03 4.8E-04 9
rs2234711
IFNGR1
0.827 0.080 6 137219383 5 prime UTR variant A/G snv 0.43 6
rs3091307
TH2LCRR
0.925 0.160 5 132653444 intron variant A/G snv 0.34 6
rs34383331
MIF-AS1
0.882 0.040 22 23895892 non coding transcript exon variant T/A snv 0.19 0.18 3
rs776022790
FYB1
0.925 0.040 5 39202836 missense variant T/C snv 4.0E-06 7.0E-06 2
rs7719175
TH2LCRR
0.925 0.120 5 132650771 intron variant T/G snv 4.4E-02 2
rs7246355
CLEC11A
1.000 0.040 19 50722987 upstream gene variant C/T snv 0.53 1