Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs669260
DDX58
0.851 0.080 9 32503442 intron variant T/A;C snv 4
rs9695310
DDX58
0.851 0.120 9 32464137 intron variant G/C snv 0.52 4
rs10945859
PRKN
0.882 0.120 6 162721570 intron variant T/C snv 0.17 3
rs1143629
IL1B
0.882 0.160 2 112835941 intron variant G/A snv 0.60 3
rs11881222
IFNL3
0.925 0.080 19 39244283 intron variant A/G snv 0.30 3
rs13220495
BTN3A3
0.925 0.160 6 26441412 intron variant C/T snv 5.3E-02 3
rs1634323
TLR7
0.882 0.200 X 12870008 intron variant A/G snv 0.11 3
rs179019
TLR7
0.882 0.160 X 12871850 intron variant A/C;T snv 3
rs2237062
CXCL14
0.882 0.120 5 135576874 intron variant G/C snv 0.26 3
rs2280964
CXCR3
0.882 0.200 X 71618204 intron variant C/A;G;T snv 3
rs538399
IGFBP4
0.925 0.120 17 40454413 intron variant A/G snv 0.33 3
rs6051702
C20orf194
0.882 0.120 20 3271278 intron variant A/C snv 0.19 3
rs730775
NFKBIE
1.000 0.080 6 44264337 intron variant A/G snv 0.36 3
rs760370
SLC29A1
0.925 0.120 6 44233216 intron variant A/G snv 0.36 3
rs12186731
HAVCR2
0.925 0.120 5 157110905 intron variant C/T snv 0.11 2
rs1297986
LINC00636
1.000 0.080 3 107912675 intron variant A/G snv 2
rs13126816
TLR3
0.925 0.200 4 186073024 intron variant G/A snv 0.21 2
rs13170556
HAVCR2
0.925 0.120 5 157095577 intron variant T/C snv 0.13 2
rs1474358
C2orf88
0.925 0.120 2 190145376 intron variant T/C snv 5.3E-03 2
rs179009
TLR7
0.925 0.160 X 12885361 intron variant A/G;T snv 2
rs2069707
IFNG ; IFNG-AS1
0.925 0.120 12 68160508 intron variant G/A;C snv 2
rs2071469
HLA-DOB
0.925 0.200 6 32817006 intron variant C/A;G;T snv 2
rs2629751
GLT8D2
0.925 0.120 12 104028030 intron variant A/G snv 0.36 2
rs2857009
TNXB
1.000 0.080 6 32051969 intron variant G/C snv 0.25 2
rs3017887
NOX4
0.925 0.120 11 89492920 intron variant A/C snv 0.81 2