Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800872
IL19 ; IL10
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs1800896
IL19 ; IL10
0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs1800871
IL19 ; IL10
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 72
rs1205
CRP
0.602 0.680 1 159712443 3 prime UTR variant C/T snv 0.30 46
rs421016
GBA
0.683 0.440 1 155235252 missense variant A/C;G snv 8.0E-06; 1.3E-03 30
rs1065489
CFH
0.695 0.440 1 196740644 missense variant G/T snv 0.20 0.15 19
rs3091244
CRP
0.724 0.280 1 159714875 upstream gene variant G/A;T snv 17
rs2808630 0.742 0.240 1 159711078 downstream gene variant C/T snv 0.77 13
rs12048215
NLRP3
0.882 0.160 1 247421289 intron variant A/G snv 0.11 3
rs1764390
LOC105378642 ; GJA4 ; SMIM12
0.882 0.160 1 34794360 missense variant A/C;G;T snv 0.61 0.69 3
rs2027432
NLRP3
0.882 0.160 1 247415139 upstream gene variant A/G;T snv 3
rs17602729
AMPD1
0.925 0.080 1 114693436 stop gained G/A;T snv 8.6E-02 2
rs1891320 0.925 0.080 1 19970618 upstream gene variant C/T snv 0.20 2
rs5744105
TLR5
0.925 0.080 1 223142735 intron variant G/C snv 0.57 2
rs231775
CTLA4
0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs16944
IL1B
0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs1143634
IL1B
0.597 0.680 2 112832813 synonymous variant G/A snv 0.19 0.19 52
rs1143627
IL1B
0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56 47
rs1143643
IL1B
0.790 0.320 2 112830725 intron variant C/T snv 0.29 10
rs11568821
LOC105373977 ; PDCD1
0.827 0.200 2 241851760 intron variant C/G;T snv 10
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
rs1524668
ADAM17
0.851 0.160 2 9557243 upstream gene variant A/C snv 0.64 4
rs11684747
ADAM17
0.925 0.080 2 9557042 upstream gene variant A/G snv 0.19 2