Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2569190
CD14 ; TMCO6
0.620 0.560 5 140633331 intron variant A/G snv 0.57 39
rs1333048
CDKN2B-AS1
0.683 0.320 9 22125348 intron variant A/C snv 0.44 24
rs1333042
CDKN2B-AS1
0.827 0.120 9 22103814 intron variant A/G snv 0.63 7
rs6596473
SLC23A1
0.807 0.120 5 139374887 intron variant G/C;T snv 7
rs496892
CDKN2B-AS1
0.827 0.160 9 22024352 intron variant C/T snv 0.40 6
rs4252120
PLG
0.827 0.080 6 160722576 intron variant T/C;G snv 0.21 5
rs1342913
BRINP3
0.851 0.040 1 190151895 intron variant G/A snv 0.61 4
rs1537415
GLT6D1
0.851 0.040 9 135637876 intron variant G/C snv 0.36 4
rs2981573
IL20
0.882 0.160 1 206867232 intron variant G/A snv 0.77 4
rs6667202
IL19
0.882 0.120 1 206783747 intron variant C/A;T snv 4
rs13005285
ATG16L1
0.882 0.080 2 233286311 intron variant T/G snv 0.56 3
rs2241879
SCARNA5 ; ATG16L1
0.882 0.080 2 233274822 intron variant G/A snv 0.45 0.44 3
rs2679895
TGFBRAP1
0.882 0.080 2 105290023 intron variant C/A;G snv 3
rs1247559
LOC105378091
0.925 0.040 6 160782724 intron variant C/T snv 0.17 2
rs3218974
IL1R2
0.925 0.040 2 102024409 intron variant A/G snv 0.27 2
rs4284742
SIGLEC5
0.925 0.040 19 51628480 intron variant A/G snv 0.78 2
rs61815643
IL19
0.925 0.040 1 206782771 intron variant G/A;T snv 2
rs1122900 1.000 0.040 5 36689079 intron variant A/C snv 0.42 1
rs574301770
ZNF136
0.925 0.040 19 12186844 stop gained C/G;T snv 8.0E-05 2
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
rs854560
PON1
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs5743708
TLR2
0.525 0.800 4 153705165 missense variant G/A snv 1.7E-02 1.8E-02 98
rs1048943
CYP1A1
0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 88
rs763780
IL17F
0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02 87