Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2857656
CCL2
0.851 0.120 17 34254988 upstream gene variant G/A;C snv 5
rs4957796
FER
0.851 0.120 5 109066439 intron variant T/C snv 0.16 5
rs9770242
NAMPT
0.851 0.240 7 106285885 5 prime UTR variant C/A snv 0.79 5
rs1524668
ADAM17
0.851 0.160 2 9557243 upstream gene variant A/C snv 0.64 4
rs2563298
TMCO6 ; CD14
0.851 0.200 5 140631730 3 prime UTR variant C/A snv 0.26 4
rs368287711
IL10RA
0.851 0.120 11 117989554 missense variant C/A;T snv 2.0E-05; 2.4E-05 4
rs11568821
LOC105373977 ; PDCD1
0.827 0.200 2 241851760 intron variant C/G;T snv 10
rs1126647
CXCL8
0.827 0.160 4 73743328 3 prime UTR variant A/T snv 0.31 8
rs121918094
TTR
0.827 0.280 18 31592921 missense variant T/C snv 8
rs212388
LOC112267968 ; LOC105378083
0.827 0.240 6 159069404 intron variant C/G;T snv 8
rs4358188
BPI
0.827 0.160 20 38318446 missense variant G/A;C snv 0.46 7
rs2297630
CXCL12
0.827 0.160 10 44376100 intron variant G/A;T snv 0.21 6
rs842647
REL
0.827 0.400 2 60892336 intron variant G/A snv 0.62 6
rs12692386
ADAM17
0.827 0.160 2 9555777 5 prime UTR variant A/G snv 0.72 5
rs13137
VMP1 ; MIR21
0.827 0.160 17 59841670 3 prime UTR variant A/T snv 0.18 5
rs2234246
TREM1
0.827 0.240 6 41276002 3 prime UTR variant C/T snv 0.44 5
rs1799768
SERPINE1
0.807 0.360 7 101126425 upstream gene variant -/A;C ins 6
rs353291
CARMN ; MIR145
0.807 0.200 5 149431183 non coding transcript exon variant T/C snv 0.35 6
rs1143643
IL1B
0.790 0.320 2 112830725 intron variant C/T snv 0.29 10
rs414171
MAPKAPK3 ; CISH
0.790 0.200 3 50612068 5 prime UTR variant A/G;T snv 9
rs4648068
NFKB1
0.790 0.240 4 102597148 intron variant A/G snv 0.31 9
rs11465996
LY96
0.790 0.240 8 73989727 upstream gene variant C/G snv 0.25 7
rs34557412
TNFRSF13B
0.763 0.240 17 16948873 missense variant A/G snv 3.5E-03 3.9E-03 15
rs10865710
PPARG
0.763 0.360 3 12311699 intron variant C/G snv 0.25 13
rs17281995
CD86
0.763 0.360 3 122120794 3 prime UTR variant G/A;C snv 11