Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9695310
DDX58
0.851 0.120 9 32464137 intron variant G/C snv 0.52 4
rs965469
C20orf194
1.000 0.080 20 3400902 intron variant T/C snv 0.20 1
rs9461776
HLA-DRB1
0.763 0.240 6 32607958 intergenic variant A/G snv 8.8E-02 11
rs9275572 0.724 0.360 6 32711222 upstream gene variant A/G;T snv 15
rs8878
ART3 ; CXCL10
0.827 0.280 4 76021147 3 prime UTR variant A/C;G snv 5
rs8109886 1.000 0.080 19 39252122 upstream gene variant C/A snv 0.53 1
rs8103142
IFNL3
0.882 0.120 19 39244466 missense variant T/C snv 0.29 0.40 4
rs8099917 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 60
rs7944926
NADSYN1
0.807 0.200 11 71454579 intron variant A/G snv 0.54 7
rs758564400
REN
0.925 0.120 1 204156683 missense variant A/G snv 4.0E-06 5
rs738409
PNPLA3
0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 88
rs7270101
ITPA
0.776 0.200 20 3213247 intron variant A/C snv 8.7E-02 9.7E-02 10
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs6897932
IL7R
0.683 0.560 5 35874473 missense variant C/T snv 0.23 0.21 25
rs641738
LOC112268246 ; TMC4 ; MBOAT7
0.689 0.320 19 54173068 missense variant T/A;C;G snv 22
rs6139030
ITPA
1.000 0.080 20 3207087 upstream gene variant T/C snv 8.6E-02 1
rs6051702
C20orf194
0.882 0.120 20 3271278 intron variant A/C snv 0.19 3
rs5998152
DEPDC5
0.827 0.160 22 31867176 intron variant T/C snv 0.37 5
rs58542926
TM6SF2
0.630 0.440 19 19268740 missense variant C/T snv 6.5E-02 5.8E-02 42
rs5743708
TLR2
0.525 0.800 4 153705165 missense variant G/A snv 1.7E-02 1.8E-02 98
rs5743704
TLR2
0.763 0.240 4 153704799 missense variant C/A snv 2.8E-02 2.8E-02 9
rs4969170
LOC101928674
0.752 0.440 17 78364457 intron variant A/C;G snv 0.54 11
rs4969168
SOCS3
0.790 0.480 17 78357712 3 prime UTR variant A/G snv 0.71 7
rs4950928
CHI3L1
0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv 33
rs4803223 1.000 0.080 19 39255579 upstream gene variant A/G snv 0.13 1