Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7270101
ITPA
0.776 0.200 20 3213247 intron variant A/C snv 8.7E-02 9.7E-02 10
rs16851720
RNF7
0.827 0.120 3 141744456 intron variant A/C snv 0.21 5
rs6051702
C20orf194
0.882 0.120 20 3271278 intron variant A/C snv 0.19 3
rs1470452230
PAEP
0.925 0.120 9 135561895 missense variant A/C snv 7.0E-06 2
rs12972991 1.000 0.080 19 39241107 upstream gene variant A/C snv 0.19 1
rs4969170
LOC101928674
0.752 0.440 17 78364457 intron variant A/C;G snv 0.54 11
rs8878
ART3 ; CXCL10
0.827 0.280 4 76021147 3 prime UTR variant A/C;G snv 5
rs2287622
ABCB11
0.724 0.240 2 168973818 missense variant A/C;G;T snv 0.57 16
rs11697186
DDRGK1
1.000 0.080 20 3204477 intron variant A/C;T snv 7.0E-02 1
rs12952093
LOC101928674
1.000 0.080 17 78367559 intron variant A/C;T snv 1
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs1800469
B9D2 ; TGFB1
0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs2569190
CD14 ; TMCO6
0.620 0.560 5 140633331 intron variant A/G snv 0.57 39
rs4444903
EGF
0.630 0.360 4 109912954 5 prime UTR variant A/G snv 0.51 35
rs10741657
CYP2R1
0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 34
rs12980275 0.701 0.360 19 39241143 upstream gene variant A/G snv 0.36 23
rs9461776
HLA-DRB1
0.763 0.240 6 32607958 intergenic variant A/G snv 8.8E-02 11
rs4374383
MERTK
0.776 0.200 2 112013193 intron variant A/G snv 0.58 10
rs1993116
CYP2R1
0.827 0.200 11 14888688 intron variant A/G snv 0.65 8
rs4969168
SOCS3
0.790 0.480 17 78357712 3 prime UTR variant A/G snv 0.71 7
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
rs11506105
EGFR
0.851 0.160 7 55152484 intron variant A/G snv 0.59 4
rs10789491
EFCAB14
1.000 0.080 1 46713638 intron variant A/G snv 0.80 1