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
rs10774625
ATXN2
0.763 0.320 12 111472415 intron variant A/G snv 0.66 13
rs8067378 0.752 0.240 17 39895095 regulatory region variant A/G snv 0.50 12
rs17622378
IRF1-AS1
0.790 0.200 5 132442760 intron variant A/G snv 0.28 8
rs569108
MS4A2
0.790 0.200 11 60095631 missense variant A/G snv 4.7E-02 7.3E-02 8
rs1295685
TH2LCRR ; IL13
0.790 0.160 5 132660753 3 prime UTR variant A/G snv 0.81 7
rs17454584 0.851 0.080 4 122432277 downstream gene variant A/G snv 0.17 6
rs479844 0.851 0.160 11 65784486 upstream gene variant A/G snv 0.44 6
rs17144046 0.882 0.120 10 8564051 intergenic variant A/G snv 0.28 4
rs9357733
EFHC1
0.851 0.160 6 52427338 intron variant A/G snv 0.19 4
rs9391997
IRF4
0.851 0.160 6 409119 3 prime UTR variant A/G snv 0.38 4
rs13277355 0.882 0.120 8 127765473 intergenic variant A/G snv 0.71 3
rs2280091
ADAM33
0.882 0.080 20 3669587 missense variant A/G snv 0.13 0.14 3
rs449454
NDFIP1
0.925 0.080 5 142153497 3 prime UTR variant A/G snv 0.65 0.68 3
rs7518129
TNFSF4
0.882 0.120 1 173194429 intron variant A/G snv 0.47 3
rs7625643
ZBTB38
0.925 0.080 3 141431184 intron variant A/G snv 0.51 3
rs7734635 0.925 0.080 5 110823145 intergenic variant A/G snv 0.30 3
rs10044254
FBXL7
0.925 0.080 5 15783487 intron variant A/G snv 0.25 2
rs114444221
HLA-B
0.925 0.080 6 31335547 intron variant A/G snv 0.18 2
rs12551256
LOC107987046 ; IL33
0.925 0.080 9 6231239 intron variant A/G snv 0.40 2
rs12964116
SERPINB7
0.925 0.080 18 63775385 5 prime UTR variant A/G snv 3.0E-02 2
rs1617333
CD247
0.925 0.080 1 167467033 intron variant A/G snv 0.27 2
rs2234678
IL1RN
0.925 0.080 2 113117988 5 prime UTR variant A/G snv 0.25 0.21 2
rs55661102
LPP
0.925 0.080 3 188683350 intron variant A/G snv 0.13 2
rs78037977 0.925 0.120 1 172746562 upstream gene variant A/G snv 7.9E-02 2