Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs35068180
MMP3
0.851 0.040 11 102845217 upstream gene variant A/-;AA delins 5
rs1333048
CDKN2B-AS1
0.683 0.320 9 22125348 intron variant A/C snv 0.44 24
rs1122900 1.000 0.040 5 36689079 intron variant A/C snv 0.42 1
rs1042229
FPR1
0.790 0.280 19 51746419 missense variant A/C;G snv 0.32; 0.13 7
rs854560
PON1
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs2569190
CD14 ; TMCO6
0.620 0.560 5 140633331 intron variant A/G snv 0.57 39
rs2241880
SCARNA5 ; ATG16L1
0.627 0.600 2 233274722 missense variant A/G snv 0.45 0.44 37
rs1333042
CDKN2B-AS1
0.827 0.120 9 22103814 intron variant A/G snv 0.63 7
rs3218977
IL1R2
0.807 0.240 2 102024739 3 prime UTR variant A/G snv 0.14 6
rs3218974
IL1R2
0.925 0.040 2 102024409 intron variant A/G snv 0.27 2
rs3819370
IL1R2
0.925 0.040 2 102016112 non coding transcript exon variant A/G snv 0.17 2
rs4284742
SIGLEC5
0.925 0.040 19 51628480 intron variant A/G snv 0.78 2
rs779229249
GPRC6A
0.925 0.040 6 116807037 missense variant A/G snv 4.0E-06 2
rs2978951 1.000 0.040 8 6965773 downstream gene variant A/G snv 0.60 1
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs4073
CXCL8
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 64
rs1800630
TNF ; LOC100287329 ; LTA
0.701 0.480 6 31574699 upstream gene variant C/A snv 0.14 17
rs2679895
TGFBRAP1
0.882 0.080 2 105290023 intron variant C/A;G snv 3
rs6667202
IL19
0.882 0.120 1 206783747 intron variant C/A;T snv 4
rs72821893
KRT25
0.925 0.040 17 40751196 missense variant C/A;T snv 1.4E-02 2
rs1800972
DEFB1
0.708 0.440 8 6877901 5 prime UTR variant C/G;T snv 0.79 16
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
rs4986791
TLR4
0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs1800450
MBL2
0.662 0.640 10 52771475 missense variant C/T snv 0.14 0.11 26