Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs1043210477
GPX1
0.701 0.520 3 49358250 missense variant G/A snv 19
rs1045411
HMGB1
0.708 0.360 13 30459095 3 prime UTR variant C/T snv 0.20 18
rs10506481
MIR6502 ; IRAK3
0.882 0.080 12 66250331 3 prime UTR variant T/C snv 9.0E-02 3
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 72
rs1065489
CFH
0.695 0.440 1 196740644 missense variant G/T snv 0.20 0.15 19
rs10865710
PPARG
0.763 0.360 3 12311699 intron variant C/G snv 0.25 13
rs11137480
S1PR3 ; C9orf47
0.882 0.120 9 88989662 upstream gene variant G/C snv 0.37 3
rs11216153
APOA1-AS
0.925 0.080 11 116834384 upstream gene variant G/T snv 0.16 2
rs1126647
CXCL8
0.827 0.160 4 73743328 3 prime UTR variant A/T snv 0.31 8
rs1129055
CD86
0.724 0.400 3 122119472 missense variant G/A snv 0.30 0.25 15
rs1143627
IL1B
0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56 47
rs1143634
IL1B
0.597 0.680 2 112832813 synonymous variant G/A snv 0.19 0.19 52
rs1143643
IL1B
0.790 0.320 2 112830725 intron variant C/T snv 0.29 10
rs11465996
LY96
0.790 0.240 8 73989727 upstream gene variant C/G snv 0.25 7
rs11536889
TLR4
0.658 0.560 9 117715853 3 prime UTR variant G/C snv 0.11 27
rs1153879
STAG1
0.925 0.080 3 136392816 intron variant G/T snv 2
rs11568821
LOC105373977 ; PDCD1
0.827 0.200 2 241851760 intron variant C/G;T snv 10
rs11666254
FPR2 ; FPR1
0.925 0.080 19 51759909 intron variant A/G snv 0.28 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
rs12048215
NLRP3
0.882 0.160 1 247421289 intron variant A/G snv 0.11 3
rs1205
CRP
0.602 0.680 1 159712443 3 prime UTR variant C/T snv 0.30 46
rs121917864
TLR2
0.645 0.520 4 153704936 missense variant C/T snv 8.8E-05 9.8E-05 31
rs121918094
TTR
0.827 0.280 18 31592921 missense variant T/C snv 8