Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11236797 0.790 0.200 11 76588605 upstream gene variant C/A snv 0.39 8
rs11264799
FCRL3
0.851 0.240 1 157700967 upstream gene variant C/T snv 0.28 6
rs1127354
ITPA
0.667 0.400 20 3213196 missense variant C/A;G snv 7.5E-02 26
rs1128503
ABCB1
0.564 0.760 7 87550285 synonymous variant A/G snv 0.54 0.63 64
rs113010081 0.925 0.160 3 46415921 downstream gene variant T/C snv 7.3E-02 3
rs113653754
HLA-DQB1-AS1
0.925 0.040 6 32658495 upstream gene variant C/A snv 3
rs1142345
TPMT
0.776 0.280 6 18130687 missense variant T/C;G snv 3.7E-02 9
rs1143627
IL1B
0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56 47
rs1143634
IL1B
0.597 0.680 2 112832813 synonymous variant G/A snv 0.19 0.19 52
rs11465797
IL23R ; C1orf141
1.000 0.040 1 67200769 missense variant C/A snv 2
rs11548656
PLCG2
1.000 0.040 16 81883307 missense variant A/G snv 2.5E-02 2.7E-02 2
rs11554257 1.000 0.040 9 114842790 upstream gene variant T/C snv 0.13 2
rs11554495
KRT8
0.701 0.240 12 52904798 missense variant C/A snv 4.9E-03 5.4E-03 19
rs11564258
MUC19 ; LOC105369736
1.000 0.040 12 40398498 intron variant G/A snv 3.1E-02 2
rs11581607
IL23R
0.925 0.040 1 67242007 intron variant G/A snv 4.6E-02 4
rs11612508
DUSP16
12 12504579 intron variant A/G snv 0.22 1
rs11614178
IFNG-AS1 ; LOC107984526
0.827 0.120 12 68114342 intron variant G/A;T snv 0.26 6
rs11614913
HOXC6 ; MIR196A2
0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs116392568
HLA-B ; LOC112267902
1.000 0.040 6 31306603 intron variant T/C snv 2
rs11641016 16 85981275 intron variant C/G snv 0.18 1
rs11641184
LITAF
0.925 0.040 16 11610795 intron variant C/A snv 0.36 3
rs11672983 1.000 0.040 19 54871595 upstream gene variant G/A snv 0.35 2
rs11677953 2 218256940 non coding transcript exon variant G/A snv 0.36 1
rs11681525
TEX41
1.000 0.040 2 144734815 intron variant C/G snv 5.9E-02 2
rs116855232
NUDT15
0.742 0.400 13 48045719 missense variant C/T snv 2.8E-02 1.1E-02 12