Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs1051931
PLA2G7
0.708 0.400 6 46705206 missense variant A/G snv 0.81 0.79 19
rs2229238
IL6R
0.851 0.080 1 154465420 3 prime UTR variant T/A;C snv 0.80 5
rs2298566
SNX19
0.827 0.040 11 130880747 missense variant A/C;T snv 0.77; 4.0E-06 5
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1883832
CD40
0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80 52
rs4142986
COL15A1
0.925 0.040 9 99052344 intron variant C/A;G;T snv 1.1E-04; 0.75; 4.0E-06 2
rs5743810
TLR6 ; TLR1
0.689 0.360 4 38828729 missense variant A/G snv 0.73 0.72 21
rs1799883
FABP2
0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 36
rs2910164
MIR3142HG ; MIR146A
0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs4673
CYBA
0.653 0.600 16 88646828 missense variant A/G;T snv 0.70 32
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 72
rs17465637
MIA3
0.790 0.200 1 222650187 intron variant A/C;G;T snv 0.64; 6.4E-06 11
rs5882
CETP
0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 35
rs9370867
MYLIP
0.827 0.120 6 16145094 missense variant A/G snv 0.60 0.63 7
rs5351
EDNRB-AS1 ; EDNRB
0.807 0.240 13 77901178 synonymous variant T/C;G snv 0.57 7
rs4523
TBXA2R
0.776 0.280 19 3595796 missense variant A/G snv 0.56 0.66 8
rs2536512
SOD3
0.752 0.280 4 24799693 missense variant G/A;T snv 0.55 14
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs1137101
LEPR
0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs5182
AGTR1
0.742 0.160 3 148741608 synonymous variant C/T snv 0.49 0.41 16
rs17611
C5
0.732 0.480 9 121006922 missense variant C/T snv 0.47 0.36 14
rs2277680
CXCL16
0.776 0.160 17 4735268 missense variant G/A snv 0.47 0.41 10
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs5498
ICAM4 ; ICAM1
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99