Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs12980275 0.701 0.360 19 39241143 upstream gene variant A/G snv 0.36 23
rs4696480
TLR2
0.716 0.400 4 153685974 intron variant T/A snv 0.45 19
rs3740066
ABCC2
0.724 0.440 10 99844450 missense variant C/G;T snv 2.4E-05; 0.34 20
rs352139
TLR9
0.732 0.320 3 52224356 intron variant T/C snv 0.51 0.54 18
rs368234815
IFNL4
0.742 0.280 19 39248514 frameshift variant TT/G;T delins 15
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
rs7270101
ITPA
0.776 0.200 20 3213247 intron variant A/C snv 8.7E-02 9.7E-02 10
rs1898830
TLR2
0.807 0.280 4 153687301 intron variant A/G snv 0.30 10
rs12583006
TNFSF13B
0.807 0.320 13 108285104 intron variant T/A snv 0.21 8
rs10853728 0.851 0.160 19 39254506 downstream gene variant C/A;G;T snv 5
rs4803217
IFNL3
0.882 0.120 19 39243580 3 prime UTR variant C/A snv 0.39 4
rs1879026
TLR3
1.000 0.080 4 186079167 intron variant G/C;T snv 3
rs17879702
HLA-DRB1
1.000 0.080 6 32584346 missense variant G/A snv 3.2E-02 5.7E-02 2
rs2237061
CXCL14
1.000 0.080 5 135576640 intron variant C/T snv 8.4E-02 2