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
rs854560
PON1
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs1800972
DEFB1
0.708 0.440 8 6877901 5 prime UTR variant C/G;T snv 0.79 16
rs80338962
SCN4A
0.742 0.240 17 63941508 missense variant T/C snv 13
rs1042229
FPR1
0.790 0.280 19 51746419 missense variant A/C;G snv 0.32; 0.13 7
rs6596473
SLC23A1
0.807 0.120 5 139374887 intron variant G/C;T snv 7
rs35068180
MMP3
0.851 0.040 11 102845217 upstream gene variant A/-;AA delins 5
rs3811046
IL37
0.851 0.160 2 112913801 missense variant G/A;T snv 4.0E-06; 0.71 5
rs4252120
PLG
0.827 0.080 6 160722576 intron variant T/C;G snv 0.21 5
rs6667202
IL19
0.882 0.120 1 206783747 intron variant C/A;T snv 4
rs104894211
CTSC
0.882 0.120 11 88294358 missense variant T/C snv 1.2E-05 3
rs2679895
TGFBRAP1
0.882 0.080 2 105290023 intron variant C/A;G snv 3
rs2070745
FPR1
0.925 0.040 19 51746694 missense variant C/G;T snv 0.40; 1.2E-05 2
rs574301770
ZNF136
0.925 0.040 19 12186844 stop gained C/G;T snv 8.0E-05 2
rs61815643
IL19
0.925 0.040 1 206782771 intron variant G/A;T snv 2
rs72821893
KRT25
0.925 0.040 17 40751196 missense variant C/A;T snv 1.4E-02 2
rs779229249
GPRC6A
0.925 0.040 6 116807037 missense variant A/G snv 4.0E-06 2
rs782383264
ELN
0.925 0.040 7 74051750 missense variant G/A snv 1.2E-05 2
rs536714306
ADGRG6
0.925 0.040 6 142419955 missense variant G/A snv 9.2E-05 2.8E-05 2
rs142548867
EEFSEC
0.925 0.040 3 128264663 missense variant C/T snv 1.8E-03 6.8E-04 2
rs145616324
SMPD3
0.925 0.040 16 68371770 missense variant G/A snv 3.7E-03 1.3E-03 2
rs104895464
NOD2
0.925 0.040 16 50712283 missense variant G/A snv 1.6E-03 1.3E-03 2
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
rs4986791
TLR4
0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182