Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs1800470
TGFB1
0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs3775291
TLR3
0.602 0.640 4 186082920 missense variant C/G;T snv 1.2E-04; 0.28 51
rs641738
LOC112268246 ; TMC4 ; MBOAT7
0.689 0.320 19 54173068 missense variant T/A;C;G snv 22
rs35761398
CNR2
0.701 0.520 1 23875429 missense variant TT/CC mnv 19
rs368234815
IFNL4
0.742 0.280 19 39248514 frameshift variant TT/G;T delins 15
rs3775290
TLR3
0.742 0.280 4 186083063 missense variant C/A;T snv 0.30 15
rs3811381
CR1
0.763 0.240 1 207616743 missense variant C/A;G snv 8.0E-06; 0.24 11
rs120074192
KCNQ1
0.763 0.120 11 2527959 missense variant A/G snv 10
rs2293152
STAT3
0.763 0.480 17 42329511 intron variant G/A;C;T snv 2.8E-05; 0.59; 1.6E-05 10
rs7453920
HLA-DQB2
0.752 0.440 6 32762235 intron variant A/G;T snv 10
rs9332739
CYP21A2 ; C2-AS1 ; C2
0.763 0.360 6 31936027 missense variant G/A;C snv 4.1E-06; 3.9E-02 10
rs414171
MAPKAPK3 ; CISH
0.790 0.200 3 50612068 5 prime UTR variant A/G;T snv 9
rs1805011
IL4R
0.776 0.320 16 27362551 missense variant A/C;G;T snv 0.13; 1.2E-04; 3.6E-05 8
rs10853728 0.851 0.160 19 39254506 downstream gene variant C/A;G;T snv 5
rs10465885
LOC102723321 ; GJA5
0.882 0.080 1 147760632 intron variant T/A;C snv 4
rs6715787
EPAS1
0.851 0.200 2 46349033 intron variant C/G;T snv 4
rs9277542
HLA-DPB1
0.851 0.280 6 33087470 3 prime UTR variant T/A;C snv 4
rs3747206
PNPLA3
0.882 0.160 22 43928850 synonymous variant C/T snv 3
rs757537938
C2 ; C2-AS1 ; CYP21A2
0.882 0.200 6 31943672 missense variant A/C snv 4.1E-06 3
rs142346548
IFNL3
0.925 0.160 19 39244145 missense variant G/A snv 4.0E-06 2
rs17408553
HLA-C ; HLA-B
0.925 0.080 6 31271630 missense variant G/A;T snv 0.37 2
rs179009
TLR7
0.925 0.160 X 12885361 intron variant A/G;T snv 2
rs1056744559
TLR4
1.000 0.080 9 117713974 stop gained C/G;T snv 4.0E-06; 2.8E-05 1
rs1265163
POU5F1 ; TCF19
1.000 0.080 6 31166310 missense variant C/G;T snv 0.14; 7.2E-06 1