Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12979860
IFNL4
0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs187084
TLR9
0.641 0.480 3 52227015 intron variant A/G snv 0.38 36
rs4696480
TLR2
0.716 0.400 4 153685974 intron variant T/A snv 0.45 19
rs352139
TLR9
0.732 0.320 3 52224356 intron variant T/C snv 0.51 0.54 18
rs2149356
TLR4
0.742 0.360 9 117711921 intron variant T/G snv 0.54 14
rs9514828
TNFSF13B
0.752 0.440 13 108269025 intron variant C/T snv 0.35 12
rs1898830
TLR2
0.807 0.280 4 153687301 intron variant A/G snv 0.30 10
rs7270101
ITPA
0.776 0.200 20 3213247 intron variant A/C snv 8.7E-02 9.7E-02 10
rs12583006
TNFSF13B
0.807 0.320 13 108285104 intron variant T/A snv 0.21 8
rs1879026
TLR3
1.000 0.080 4 186079167 intron variant G/C;T snv 3
rs2237061
CXCL14
1.000 0.080 5 135576640 intron variant C/T snv 8.4E-02 2
rs10484389
CASC15
6 22075033 intron variant C/T snv 6.0E-02 1
rs11025185
NAV2
11 19572259 intron variant G/A snv 2.4E-03 1
rs1432133
GABRG3
15 26983199 intron variant A/G;T snv 1
rs4683336
KRBOX1 ; ACKR2
3 42818461 intron variant C/T snv 0.61 1
rs8014067
SYT16
14 62086539 intron variant A/T snv 0.79 1
rs2174866
LOC107983981
15 53172023 intergenic variant A/T snv 6.2E-02 1
rs7518687
LOC105371604
1 168663745 intergenic variant A/T snv 0.22 1
rs9522267 13 111544020 intergenic variant G/A snv 0.32 1
rs1042522
TP53
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs878854066
TP53
0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs738409
PNPLA3
0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 88
rs1127354
ITPA
0.667 0.400 20 3213196 missense variant C/A;G snv 7.5E-02 26
rs641738
LOC112268246 ; TMC4 ; MBOAT7
0.689 0.320 19 54173068 missense variant T/A;C;G snv 22