Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12252
IFITM3
0.695 0.240 11 320772 splice region variant A/G snv 0.13 0.13 23
rs12212067
FOXO3
0.716 0.320 6 108659993 intron variant T/G snv 0.14 20
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs8099917 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 60
rs4553808
CTLA4
0.672 0.320 2 203866282 upstream gene variant A/G;T snv 0.16 28
rs179008
TLR7
0.763 0.360 X 12885540 missense variant A/C;T snv 0.18 0.18 14
rs7269320
MAVS
20 3865750 missense variant C/T snv 0.16 0.21 1
rs3136558
IL1B
1.000 2 112833698 intron variant A/G snv 0.21 4
rs738409
PNPLA3
0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 88
rs4804803
CD209
0.732 0.360 19 7747847 upstream gene variant A/G snv 0.26 15
rs12487066
LOC105374027
1.000 0.080 3 106193283 intron variant T/C snv 0.28 2
rs486907
RNASEL
0.667 0.360 1 182585422 missense variant C/T snv 0.31 0.28 32
rs11614913
HOXC6 ; MIR196A2
0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs12980275 0.701 0.360 19 39241143 upstream gene variant A/G snv 0.36 23
rs12979860
IFNL4
0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs1990760
IFIH1
0.672 0.480 2 162267541 missense variant C/T snv 0.50 0.45 33
rs16944
IL1B
0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92