Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs1041163
VCAM1
0.882 0.160 1 100718269 upstream gene variant T/C snv 0.18 3
rs1561198
VAMP5
0.882 0.120 2 85582866 upstream gene variant C/T snv 0.52 3
rs2277438
TNFSF11
0.827 0.160 13 42581032 intron variant G/A;C snv 5
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs3764879
TLR8 ; TLR8-AS1
0.807 0.320 X 12906578 intron variant C/G snv 0.30 6
rs3853839
TLR7
0.752 0.480 X 12889539 3 prime UTR variant C/G;T snv 10
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs4986791
TLR4
0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs1927911
TLR4
0.658 0.640 9 117707776 intron variant A/G snv 0.62 28
rs11536889
TLR4
0.658 0.560 9 117715853 3 prime UTR variant G/C snv 0.11 27
rs2149356
TLR4
0.742 0.360 9 117711921 intron variant T/G snv 0.54 14
rs7873784
TLR4
0.752 0.440 9 117716658 3 prime UTR variant G/A;C;T snv 11
rs5743708
TLR2
0.525 0.800 4 153705165 missense variant G/A snv 1.7E-02 1.8E-02 98
rs5743611
TLR1
0.807 0.160 4 38798593 missense variant C/G snv 6.9E-02 7.1E-02 7
rs1800470
TGFB1
0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs1800471
TGFB1
0.597 0.840 19 41352971 missense variant C/G;T snv 5.6E-02 48
rs6885116
TENM2
0.925 0.040 5 168216540 intron variant A/G snv 0.14 2
rs953038635
SOD2
0.590 0.800 6 159692720 missense variant G/A;T snv 8.0E-06 51
rs11084095
SIGLEC5
0.925 0.040 19 51623777 intron variant G/A snv 0.30 2
rs4284742
SIGLEC5
0.925 0.040 19 51628480 intron variant A/G snv 0.78 2
rs729876
SHISA9 ; LOC107984137
0.925 0.040 16 13294921 intron variant T/C snv 0.16 2
rs5361
SELE ; C1orf112
0.623 0.720 1 169731919 missense variant T/G snv 8.3E-02; 8.0E-06 7.8E-02 47
rs1801282
PPARG
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs1805192
PPARG
0.510 0.840 3 12379739 missense variant C/G snv 121