Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1131691014
TP53
0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs7270101
ITPA
0.776 0.200 20 3213247 intron variant A/C snv 8.7E-02 9.7E-02 10
rs3746444
MIR499A ; MIR499B ; MYH7B ; LOC107985393
0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs187084
TLR9
0.641 0.480 3 52227015 intron variant A/G snv 0.38 36
rs12980275 0.701 0.360 19 39241143 upstream gene variant A/G snv 0.36 23
rs1898830
TLR2
0.807 0.280 4 153687301 intron variant A/G snv 0.30 10
rs3087943
TDP2
6 24650533 3 prime UTR variant A/G snv 0.18 1
rs1432133
GABRG3
15 26983199 intron variant A/G;T snv 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
rs8014067
SYT16
14 62086539 intron variant A/T snv 0.79 1
rs4803217
IFNL3
0.882 0.120 19 39243580 3 prime UTR variant C/A snv 0.39 4
rs17568725 5 171743637 TF binding site variant C/A snv 0.19 1
rs1127354
ITPA
0.667 0.400 20 3213196 missense variant C/A;G snv 7.5E-02 26
rs352140
TLR9
0.630 0.680 3 52222681 synonymous variant C/A;G;T snv 2.0E-05; 0.49 42
rs10853728 0.851 0.160 19 39254506 downstream gene variant C/A;G;T snv 5
rs4467099
LOC400499
16 11449038 missense variant C/A;T snv 0.66 1
rs2910164
MIR3142HG ; MIR146A
0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs738409
PNPLA3
0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 88
rs3740066
ABCC2
0.724 0.440 10 99844450 missense variant C/G;T snv 2.4E-05; 0.34 20
rs11614913
HOXC6 ; MIR196A2
0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs12979860
IFNL4
0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs9514828
TNFSF13B
0.752 0.440 13 108269025 intron variant C/T snv 0.35 12
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