Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7873784
TLR4
0.752 0.440 9 117716658 3 prime UTR variant G/A;C;T snv 11
rs10759931 0.790 0.360 9 117701869 upstream gene variant G/A;T snv 9
rs1518111
IL19 ; IL10
0.790 0.360 1 206771300 intron variant T/C snv 0.71 9
rs414171
MAPKAPK3 ; CISH
0.790 0.200 3 50612068 5 prime UTR variant A/G;T snv 9
rs10995271 0.776 0.280 10 62678726 downstream gene variant G/C snv 0.32 8
rs3021094
IL10 ; IL19
0.827 0.360 1 206771607 intron variant T/G snv 8.0E-02 8
rs1010
VAMP8
0.807 0.120 2 85581859 3 prime UTR variant T/C;G snv 7
rs11003125
MBL2
0.790 0.480 10 52772254 upstream gene variant G/C snv 0.31 7
rs2522137
MSI1
0.827 0.120 12 120342128 3 prime UTR variant T/A;C;G snv 7
rs10421768
HAMP
0.807 0.120 19 35281996 intron variant A/G snv 0.21 6
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
rs5743899
TOLLIP ; LOC105376512
0.807 0.160 11 1302334 intron variant C/T snv 0.71 6
rs11574143
VDR
0.827 0.200 12 47841134 downstream gene variant C/T snv 0.11 5
rs1800870
ALDH3A2
0.851 0.200 17 19649164 intron variant C/T snv 5
rs1978331
LTA4H
0.827 0.200 12 96015423 intron variant A/G snv 0.50 5
rs56061981
CXCL10 ; ART3
0.851 0.120 4 76023632 intron variant C/T snv 7.6E-02 5
rs1861493
IFNG ; IFNG-AS1
0.851 0.280 12 68157416 intron variant G/A snv 0.76 4
rs4988453
MYD88 ; ACAA1
0.851 0.200 3 38137763 upstream gene variant C/A;T snv 4
rs7194886 0.851 0.080 16 50691282 upstream gene variant C/T snv 0.38 4
rs897200
STAT4
0.851 0.280 2 191153045 upstream gene variant T/C snv 0.54 4
rs11168287
VDR
0.882 0.160 12 47891631 intron variant G/A snv 0.56 3
rs12998782
MARCO
0.882 0.160 2 118967804 intron variant C/T snv 0.19 3
rs2280789
LOC105371744 ; CCL5
0.925 0.080 17 35879999 intron variant A/G snv 0.16 3
rs2393799
P2RX7 ; LOC105370032
0.882 0.200 12 121132209 upstream gene variant C/A;T snv 3