Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1801275
IL4R
0.581 0.680 16 27363079 missense variant A/G snv 0.25 0.36 58
rs1051740
EPHX1
0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 56
rs3745274
CYP2B6
0.672 0.480 19 41006936 missense variant G/A;T snv 4.0E-06; 0.27 30
rs5010528
HLA-B ; HLA-C
0.827 0.240 6 31273255 intron variant A/G snv 0.15 9
rs28399499
CYP2B6
0.827 0.280 19 41012316 missense variant T/C snv 5.1E-03 2.2E-02 6
rs6500265 0.882 0.240 16 49912759 intergenic variant C/G;T snv 0.27 3
rs9933632 0.882 0.240 16 49906847 intergenic variant G/T snv 0.31 3
rs79908535
LOC105379176 ; IL4
0.882 0.280 5 132679856 missense variant G/A snv 6.8E-05 2.8E-05 3
rs41544623
MICA
0.882 0.280 6 31411083 missense variant C/T snv 3
rs137853248
HSPG2
0.925 0.080 1 21864874 missense variant C/T snv 4.3E-06 2
rs76228616
TRAF3IP2-AS1 ; TRAF3IP2
0.925 0.240 6 111601300 5 prime UTR variant G/C snv 5.8E-02 2
rs1327754652
HSPG2
1.000 0.080 1 21836802 missense variant C/T snv 5.9E-06 1.4E-05 1