Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4073
CXCL8
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 64
rs653765
ADAM10
0.763 0.240 15 58749813 upstream gene variant T/C;G snv 0.45 10
rs2234246
TREM1
0.827 0.240 6 41276002 3 prime UTR variant C/T snv 0.44 5
rs1800896
IL19 ; IL10
0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs1799946
DEFB1
0.732 0.360 8 6877909 5 prime UTR variant C/T snv 0.36 0.41 13
rs7022797
C9orf47 ; S1PR3
0.882 0.120 9 88989548 upstream gene variant T/G snv 0.38 3
rs2721068
FOXO1
0.882 0.160 13 40565575 intron variant T/C snv 0.38 4
rs187084
TLR9
0.641 0.480 3 52227015 intron variant A/G snv 0.38 36
rs11137480
S1PR3 ; C9orf47
0.882 0.120 9 88989662 upstream gene variant G/C snv 0.37 3
rs353291
CARMN ; MIR145
0.807 0.200 5 149431183 non coding transcript exon variant T/C snv 0.35 6
rs2227306
CXCL8
0.677 0.680 4 73741338 intron variant C/T snv 0.31 21
rs1126647
CXCL8
0.827 0.160 4 73743328 3 prime UTR variant A/T snv 0.31 8
rs4648068
NFKB1
0.790 0.240 4 102597148 intron variant A/G snv 0.31 9
rs1205
CRP
0.602 0.680 1 159712443 3 prime UTR variant C/T snv 0.30 46
rs1143643
IL1B
0.790 0.320 2 112830725 intron variant C/T snv 0.29 10
rs4684846
PPARG
0.882 0.080 3 12297350 intron variant A/G snv 0.28 3
rs11666254
FPR2 ; FPR1
0.925 0.080 19 51759909 intron variant A/G snv 0.28 2
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs4919510
SEMA4G ; MIR608 ; MRPL43
0.641 0.520 10 100975021 mature miRNA variant C/G snv 0.27 0.27 32
rs2563298
TMCO6 ; CD14
0.851 0.200 5 140631730 3 prime UTR variant C/A snv 0.26 4
rs1129055
CD86
0.724 0.400 3 122119472 missense variant G/A snv 0.30 0.25 15
rs10865710
PPARG
0.763 0.360 3 12311699 intron variant C/G snv 0.25 13
rs11465996
LY96
0.790 0.240 8 73989727 upstream gene variant C/G snv 0.25 7
rs12508721
IL21-AS1
0.742 0.360 4 122623509 intron variant C/T snv 0.24 11
rs61330082
NAMPT
0.732 0.320 7 106286419 upstream gene variant G/A snv 0.22 13