Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11123810
AFF3
0.925 0.200 2 100142823 intron variant T/C snv 0.37 2
rs13015714
IL18R1
0.882 0.200 2 102355405 intron variant G/T snv 0.77 3
rs917997 0.701 0.480 2 102454108 downstream gene variant T/A;C snv 20
rs2075184 0.724 0.240 2 102464132 intergenic variant T/C snv 0.78 14
rs990171 1.000 0.080 2 102470310 upstream gene variant A/C snv 0.78 2
rs1468788
SLC9A4
1.000 0.080 2 102476054 intron variant C/T snv 0.54 2
rs1799969
ICAM1
0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02 38
rs5498
ICAM4 ; ICAM1
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs9391227 1.000 0.080 6 104710759 regulatory region variant T/A snv 0.56 1
rs62131887 0.724 0.240 19 10476920 intergenic variant C/T snv 0.37 14
rs11839053 0.724 0.240 13 106410694 intergenic variant T/C snv 7.0E-02 14
rs6498114
CIITA ; LOC105371080
1.000 0.080 16 10870261 intron variant G/T snv 0.78 2
rs7104791 1.000 0.080 11 111326133 downstream gene variant T/A;C snv 1
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 41
rs187238
IL18
0.602 0.680 11 112164265 intron variant C/A;G snv 48
rs1946518
IL18
0.602 0.760 11 112164735 intron variant T/G snv 0.60 46
rs11066188
HECTD4
0.851 0.320 12 112172910 intron variant G/A;C snv 0.30; 4.1E-06 7
rs12928822
LOC105371082 ; RMI2
0.882 0.200 16 11310036 intron variant C/T snv 0.13 5
rs6679677
PHTF1
0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 26
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs4246905
TNFSF15
0.716 0.400 9 114790969 missense variant T/A;C snv 0.76 16
rs4946111 1.000 0.080 6 115663255 intergenic variant T/A;G snv 1
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs4986791
TLR4
0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182