Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs11025185
NAV2
11 19572259 intron variant G/A snv 2.4E-03 1
rs1432133
GABRG3
15 26983199 intron variant A/G;T snv 1
rs17568725 5 171743637 TF binding site variant C/A snv 0.19 1
rs2174866
LOC107983981
15 53172023 intergenic variant A/T snv 6.2E-02 1
rs3087943
TDP2
6 24650533 3 prime UTR variant A/G snv 0.18 1
rs4467099
LOC400499
16 11449038 missense variant C/A;T snv 0.66 1
rs4683336
KRBOX1 ; ACKR2
3 42818461 intron variant C/T snv 0.61 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
rs9522267 13 111544020 intergenic variant G/A snv 0.32 1
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
rs4803217
IFNL3
0.882 0.120 19 39243580 3 prime UTR variant C/A snv 0.39 4
rs10853728 0.851 0.160 19 39254506 downstream gene variant C/A;G;T snv 5
rs7270101
ITPA
0.776 0.200 20 3213247 intron variant A/C snv 8.7E-02 9.7E-02 10
rs368234815
IFNL4
0.742 0.280 19 39248514 frameshift variant TT/G;T delins 15
rs1898830
TLR2
0.807 0.280 4 153687301 intron variant A/G snv 0.30 10
rs641738
LOC112268246 ; TMC4 ; MBOAT7
0.689 0.320 19 54173068 missense variant T/A;C;G snv 22
rs352139
TLR9
0.732 0.320 3 52224356 intron variant T/C snv 0.51 0.54 18
rs12583006
TNFSF13B
0.807 0.320 13 108285104 intron variant T/A snv 0.21 8
rs12980275 0.701 0.360 19 39241143 upstream gene variant A/G snv 0.36 23
rs2149356
TLR4
0.742 0.360 9 117711921 intron variant T/G snv 0.54 14