Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800896
IL19 ; IL10
0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs1800469
B9D2 ; TGFB1
0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs187238
IL18
0.602 0.680 11 112164265 intron variant C/A;G snv 48
rs1946518
IL18
0.602 0.760 11 112164735 intron variant T/G snv 0.60 46
rs2569190
CD14 ; TMCO6
0.620 0.560 5 140633331 intron variant A/G snv 0.57 39
rs909253
LTA ; LOC100287329
0.641 0.600 6 31572536 intron variant A/G;T snv 34
rs1927911
TLR4
0.658 0.640 9 117707776 intron variant A/G snv 0.62 28
rs1333048
CDKN2B-AS1
0.683 0.320 9 22125348 intron variant A/C snv 0.44 24
rs2149356
TLR4
0.742 0.360 9 117711921 intron variant T/G snv 0.54 14
rs2234663
IL1RN
0.716 0.480 2 113130529 intron variant ATCCTGGGGAAAGTGAGGGAAATATGGACATCACATGGAACAACATCCAGGAGACTCAGGCCTCTAGGAGTAACTGGGTAGTGTGCATCCTGGGGAAAGTGAGGGAAATATGGACATCACATGGAACAACATCCAGGAGACTCAGGCCTCTAGGAGTAACTGGGTAGTGTGC/-;ATCCTGGGGAAAGTGAGGGAAATATGGACATCACATGGAACAACATCCAGGAGACTCAGGCCTCTAGGAGTAACTGGGTAGTGTGC;ATCCTGGGGAAAGTGAGGGAAATATGGACATCACATGGAACAACATCCAGGAGACTCAGGCCTCTAGGAGTAACTGGGTAGTGTGCATCCTGGGGAAAGTGAGGGAAATATGGACATCACATGGAACAACATCCAGGAGACTCAGGCCTCTAGGAGTAACTGGGTAGTGTGCATCCTGGGGAAAGTGAGGGAAATATGGACATCACATGGAACAACATCCAGGAGACTCAGGCCTCTAGGAGTAACTGGGTAGTGTGC;ATCCTGGGGAAAGTGAGGGAAATATGGACATCACATGGAACAACATCCAGGAGACTCAGGCCTCTAGGAGTAACTGGGTAGTGTGCATCCTGGGGAAAGTGAGGGAAATATGGACATCACATGGAACAACATCCAGGAGACTCAGGCCTCTAGGAGTAACTGGGTAGTGTGCATCCTGGGGAAAGTGAGGGAAATATGGACATCACATGGAACAACATCCAGGAGACTCAGGCCTCTAGGAGTAACTGGGTAGTGTGCATCCTGGGGAAAGTGAGGGAAATATGGACATCACATGGAACAACATCCAGGAGACTCAGGCCTCTAGGAGTAACTGGGTAGTGTGC delins 14
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
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
rs12032672
PKN2-AS1
0.925 0.040 1 88159953 intron variant A/C snv 0.37 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
rs992670
C5
0.882 0.120 9 121019492 intron variant G/A snv 0.52 3
rs1035029
C5
1.000 0.040 9 120980540 intron variant G/A snv 0.63 2
rs11084095
SIGLEC5
0.925 0.040 19 51623777 intron variant G/A snv 0.30 2
rs13237474 0.925 0.040 7 135816721 intron variant C/T snv 2.3E-02 2
rs2569991
LOC105376956 ; LINC02022
0.925 0.040 3 12881698 intron variant C/A snv 0.72 2