Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2808630 0.742 0.240 1 159711078 downstream gene variant C/T snv 0.77 13
rs1429638 0.925 0.080 4 73872213 downstream gene variant C/A;G snv 0.17 2
rs9529561 1.000 0.080 13 69325374 downstream gene variant A/G snv 6.3E-02 1
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs16944
IL1B
0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs4073
CXCL8
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 64
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs361525
TNF
0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 62
rs1800625
AGER ; PBX2
0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 39
rs1800624
PBX2 ; AGER
0.658 0.480 6 32184610 upstream gene variant A/G;T snv 33
rs3091244
CRP
0.724 0.280 1 159714875 upstream gene variant G/A;T snv 17
rs7096206
MBL2
0.708 0.480 10 52771925 upstream gene variant G/A;C;T snv 17
rs61330082
NAMPT
0.732 0.320 7 106286419 upstream gene variant G/A snv 0.22 13
rs510432
ATG5
0.752 0.280 6 106326155 upstream gene variant T/C snv 0.57 11
rs653765
ADAM10
0.763 0.240 15 58749813 upstream gene variant T/C;G snv 0.45 10
rs11465996
LY96
0.790 0.240 8 73989727 upstream gene variant C/G snv 0.25 7
rs1799768
SERPINE1
0.807 0.360 7 101126425 upstream gene variant -/A;C ins 6
rs2857656
CCL2
0.851 0.120 17 34254988 upstream gene variant G/A;C snv 5
rs1524668
ADAM17
0.851 0.160 2 9557243 upstream gene variant A/C snv 0.64 4
rs11137480
S1PR3 ; C9orf47
0.882 0.120 9 88989662 upstream gene variant G/C snv 0.37 3
rs2027432
NLRP3
0.882 0.160 1 247415139 upstream gene variant A/G;T snv 3
rs7022797
C9orf47 ; S1PR3
0.882 0.120 9 88989548 upstream gene variant T/G snv 0.38 3
rs11216153
APOA1-AS
0.925 0.080 11 116834384 upstream gene variant G/T snv 0.16 2
rs11684747
ADAM17
0.925 0.080 2 9557042 upstream gene variant A/G snv 0.19 2
rs11689958
ADAM17
0.925 0.080 2 9557277 upstream gene variant G/A snv 0.19 2