Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9514828
TNFSF13B
0.752 0.440 13 108269025 intron variant C/T snv 0.35 12
rs12583006
TNFSF13B
0.807 0.320 13 108285104 intron variant T/A snv 0.21 8
rs9522267 13 111544020 intergenic variant G/A snv 0.32 1
rs4467099
LOC400499
16 11449038 missense variant C/A;T snv 0.66 1
rs2149356
TLR4
0.742 0.360 9 117711921 intron variant T/G snv 0.54 14
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs2237061
CXCL14
1.000 0.080 5 135576640 intron variant C/T snv 8.4E-02 2
rs4696480
TLR2
0.716 0.400 4 153685974 intron variant T/A snv 0.45 19
rs1898830
TLR2
0.807 0.280 4 153687301 intron variant A/G snv 0.30 10
rs3804099
TLR2
0.627 0.680 4 153703504 synonymous variant T/C snv 0.40 0.48 40
rs3804100
TLR2
0.633 0.720 4 153704257 synonymous variant T/C snv 9.0E-02 6.7E-02 36
rs2910164
MIR3142HG ; MIR146A
0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs7518687
LOC105371604
1 168663745 intergenic variant A/T snv 0.22 1
rs17568725 5 171743637 TF binding site variant C/A snv 0.19 1
rs1879026
TLR3
1.000 0.080 4 186079167 intron variant G/C;T snv 3
rs11025185
NAV2
11 19572259 intron variant G/A snv 2.4E-03 1
rs10484389
CASC15
6 22075033 intron variant C/T snv 6.0E-02 1
rs1047782
TDP2
6 24650503 3 prime UTR variant T/C;G snv 1
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
rs1127354
ITPA
0.667 0.400 20 3213196 missense variant C/A;G snv 7.5E-02 26
rs7270101
ITPA
0.776 0.200 20 3213247 intron variant A/C snv 8.7E-02 9.7E-02 10
rs17879702
HLA-DRB1
1.000 0.080 6 32584346 missense variant G/A snv 3.2E-02 5.7E-02 2
rs3746444
MIR499A ; MIR499B ; MYH7B ; LOC107985393
0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs12980275 0.701 0.360 19 39241143 upstream gene variant A/G snv 0.36 23