Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs7518687
LOC105371604
1 168663745 intergenic variant A/T snv 0.22 1
rs352140
TLR9
0.630 0.680 3 52222681 synonymous variant C/A;G;T snv 2.0E-05; 0.49 42
rs187084
TLR9
0.641 0.480 3 52227015 intron variant A/G snv 0.38 36
rs352139
TLR9
0.732 0.320 3 52224356 intron variant T/C snv 0.51 0.54 18
rs4683336
KRBOX1 ; ACKR2
3 42818461 intron variant C/T snv 0.61 1
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
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
rs1879026
TLR3
1.000 0.080 4 186079167 intron variant G/C;T snv 3
rs2910164
MIR3142HG ; MIR146A
0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs2237061
CXCL14
1.000 0.080 5 135576640 intron variant C/T snv 8.4E-02 2
rs17568725 5 171743637 TF binding site variant C/A snv 0.19 1
rs17879702
HLA-DRB1
1.000 0.080 6 32584346 missense variant G/A snv 3.2E-02 5.7E-02 2
rs1047782
TDP2
6 24650503 3 prime UTR variant T/C;G snv 1
rs10484389
CASC15
6 22075033 intron variant C/T snv 6.0E-02 1
rs3087943
TDP2
6 24650533 3 prime UTR variant A/G snv 0.18 1
rs2149356
TLR4
0.742 0.360 9 117711921 intron variant T/G snv 0.54 14
rs3740066
ABCC2
0.724 0.440 10 99844450 missense variant C/G;T snv 2.4E-05; 0.34 20
rs11025185
NAV2
11 19572259 intron variant G/A snv 2.4E-03 1
rs11614913
HOXC6 ; MIR196A2
0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
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