Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2737190 0.827 0.120 9 117701903 upstream gene variant G/A snv 0.52 6
rs3764879
TLR8 ; TLR8-AS1
0.807 0.320 X 12906578 intron variant C/G snv 0.30 6
rs10484879
IL17A
0.827 0.160 6 52187159 intron variant G/A;T snv 5
rs2277438
TNFSF11
0.827 0.160 13 42581032 intron variant G/A;C snv 5
rs35068180
MMP3
0.851 0.040 11 102845217 upstream gene variant A/-;AA delins 5
rs6681231 0.882 0.120 1 186690727 intergenic variant G/C snv 0.22 5
rs11634042
ADAMTS7 ; MORF4L1
0.882 0.120 15 78813008 intron variant C/T snv 0.33 4
rs133049
MRTFA
0.882 0.080 22 40635351 intron variant A/- delins 0.82 4
rs1537415
GLT6D1
0.851 0.040 9 135637876 intron variant G/C snv 0.36 4
rs6785049
NR1I2
0.882 0.080 3 119814886 intron variant G/A;T snv 0.46 4
rs1041163
VCAM1
0.882 0.160 1 100718269 upstream gene variant T/C snv 0.18 3
rs1126580
CXCR2
0.882 0.120 2 218136243 3 prime UTR variant G/A;T snv 3
rs12032672
PKN2-AS1
0.925 0.040 1 88159953 intron variant A/C snv 0.37 3
rs1523128
NR1I2
0.882 0.080 3 119781817 5 prime UTR variant A/G snv 0.89 3
rs1561198
VAMP5
0.882 0.120 2 85582866 upstream gene variant C/T snv 0.52 3
rs2227532
CXCL8
0.882 0.120 4 73739815 upstream gene variant T/C snv 2.9E-02 3
rs2521634
LOC107986777
0.882 0.040 7 24338421 intron variant G/A;C snv 3
rs3826782
ADGRE1
0.882 0.040 19 6887725 intron variant G/A snv 8.6E-02 3
rs7762544 0.882 0.040 6 41411577 intergenic variant G/A snv 0.81 3
rs992670
C5
0.882 0.120 9 121019492 intron variant G/A snv 0.52 3
rs1027009063
KIDINS220
0.925 0.040 2 8802974 stop gained G/A snv 2
rs1035029
C5
1.000 0.040 9 120980540 intron variant G/A snv 0.63 2
rs10760187 0.925 0.040 9 121803541 intergenic variant T/A;C snv 2
rs11084095
SIGLEC5
0.925 0.040 19 51623777 intron variant G/A snv 0.30 2
rs11621969 0.925 0.040 14 75347325 intergenic variant T/C snv 0.14 2