Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4986791
TLR4
0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs5743708
TLR2
0.525 0.800 4 153705165 missense variant G/A snv 1.7E-02 1.8E-02 98
rs361525
TNF
0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 62
rs2430561
IFNG ; IFNG-AS1
0.590 0.760 12 68158742 intron variant T/A snv 0.36 50
rs1143627
IL1B
0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56 47
rs3804100
TLR2
0.633 0.720 4 153704257 synonymous variant T/C snv 9.0E-02 6.7E-02 36
rs5743836
TLR9
0.658 0.440 3 52226766 intron variant A/G snv 0.20 31
rs4833095
TLR1
0.662 0.480 4 38798089 missense variant T/C snv 0.38 0.44 28
rs12212067
FOXO3
0.716 0.320 6 108659993 intron variant T/G snv 0.14 20
rs1861494
IFNG-AS1 ; IFNG
0.716 0.400 12 68157629 intron variant C/T snv 0.75 15
rs35947132
PRF1
0.776 0.280 10 70600631 missense variant G/A snv 2.9E-02 2.9E-02 10
rs1898830
TLR2
0.807 0.280 4 153687301 intron variant A/G snv 0.30 10
rs10759931 0.790 0.360 9 117701869 upstream gene variant G/A;T snv 9
rs2234711
IFNGR1
0.827 0.080 6 137219383 5 prime UTR variant A/G snv 0.43 6
rs5743557
TLR1
0.882 0.160 4 38805206 5 prime UTR variant G/A snv 0.14 4
rs386699558
LOC107986589 ; HLA-DQA1 ; HLA-DQA2
0.882 0.080 6 32642624 missense variant GCC/ACA mnv 3
rs9272785
LOC107986589 ; HLA-DQA1 ; HLA-DQA2
0.882 0.080 6 32642624 missense variant G/A snv 0.18 8.7E-02 3
rs5743604
TLR1
0.925 0.040 4 38799664 intron variant A/G snv 0.36 3