Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6901221 0.925 0.160 6 33130499 downstream gene variant A/C snv 0.13 2
rs756440 0.925 0.160 6 33154554 intergenic variant A/G snv 0.24 2
rs6928977
AHI1
0.925 0.120 6 135305210 intron variant T/G snv 0.70 2
rs34972832
CLEC16A
0.925 0.120 16 11105081 intron variant G/A;T snv 0.14 2
rs3806624
EOMES
0.925 0.200 3 27723132 upstream gene variant A/G snv 0.61 2
rs7745098
HBS1L
1.000 0.120 6 135093866 intron variant C/G;T snv 2
rs3129223
HCG24 ; LOC105375021
0.925 0.160 6 33145420 intron variant C/T snv 0.24 2
rs3129234
HCG24 ; LOC105375021
0.925 0.160 6 33143570 upstream gene variant C/T snv 0.24 2
rs7754200
LOC105375021 ; HLA-DPA3 ; HCG24
0.925 0.160 6 33143156 intron variant A/G snv 0.24 2
rs2242660
PRRC2A
0.925 0.160 6 31629976 intron variant G/A snv 0.46 2
rs13255292
PVT1
0.925 0.120 8 128064327 intron variant C/T snv 0.24 2
rs2019960
PVT1
0.925 0.160 8 128180025 intron variant T/C snv 0.27 2
rs10881578
RXRA
0.925 0.240 9 134340689 intron variant A/G snv 0.32 2
rs12488654
TNFSF10
0.925 0.160 3 172524100 upstream gene variant G/A snv 0.16 2
rs649775 0.882 0.120 6 33716536 upstream gene variant A/G;T snv 3
rs3781093
GATA3
0.882 0.120 10 8059964 intron variant T/C snv 0.19 3
rs805294
LY6G6C ; MPIG6B
0.882 0.240 6 31720440 intron variant A/G snv 0.48 3
rs1860661
TCF3
0.882 0.120 19 1650135 intron variant A/C;G snv 6.7E-06; 0.54 3
rs4240807 0.851 0.160 16 85951755 downstream gene variant A/C snv 0.76 4
rs9296015 0.851 0.280 6 32251212 upstream gene variant G/A snv 0.22 4
rs9392017 0.851 0.160 6 442357 intergenic variant G/A;C snv 4
rs2292779
AGO2
0.851 0.320 8 140551294 intron variant G/C;T snv 0.57; 4.9E-06 4
rs35603048
BMF
0.851 0.160 15 40099764 intron variant C/A;G;T snv 4
rs73005220
CIB3
0.851 0.160 19 16161878 intron variant A/G snv 3.9E-02 4
rs6546149
DTNB
0.851 0.160 2 25406569 intron variant C/G snv 0.38 4