Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs5498
ICAM4 ; ICAM1
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs17611
C5
0.732 0.480 9 121006922 missense variant C/T snv 0.47 0.36 14
rs10818488
C5-OT1
0.776 0.360 9 120942809 regulatory region variant A/G snv 0.51 8
rs3761847
TRAF1
0.827 0.200 9 120927961 intron variant G/A snv 0.52 8
rs25681
C5
0.882 0.120 9 121017727 synonymous variant G/A snv 0.47 0.35 3
rs992670
C5
0.882 0.120 9 121019492 intron variant G/A snv 0.52 3
rs1374607932
TLR4
0.882 0.280 9 117713653 missense variant G/A snv 7.0E-06 3