Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1834306
MIR10526 ; MIR100 ; MIR100HG
0.776 0.200 11 122152479 intron variant A/G snv 0.49 9
rs2266959
UBE2L3
0.776 0.200 22 21568615 intron variant G/T snv 0.18 9
rs2280883
FOXP3
0.827 0.280 X 49252667 intron variant T/C snv 0.30 9
rs2284553
IFNGR2
0.776 0.240 21 33404389 intron variant A/G snv 0.69 9
rs430397
HSPA5
0.763 0.240 9 125238840 intron variant C/T snv 9.1E-02 0.11 9
rs7582694
STAT4
0.763 0.400 2 191105394 intron variant C/G snv 0.77 9
rs9261204
ZNRD1ASP
0.790 0.200 6 30037466 intron variant A/G snv 0.17 9
rs10168266
STAT4
0.776 0.400 2 191071078 intron variant C/T snv 0.19 8
rs12583006
TNFSF13B
0.807 0.320 13 108285104 intron variant T/A snv 0.21 8
rs4823173
PNPLA3
0.827 0.200 22 43932850 intron variant G/A snv 0.24 0.18 8
rs636832
AGO1
0.790 0.400 1 35897874 intron variant G/A snv 0.23 8
rs12663103
GPSM3
0.851 0.240 6 32193547 intron variant T/C snv 6.1E-02 7
rs17401966
KIF1B
0.790 0.280 1 10325413 intron variant A/G snv 0.24 7
rs2266961
UBE2L3
0.807 0.160 22 21574308 intron variant C/G snv 0.18 7
rs4024
AFP
0.827 0.120 4 73435667 intron variant G/A snv 0.52 7
rs6568431
ATG5
0.790 0.320 6 106140931 intron variant A/C snv 0.61 7
rs737241
AFP
0.827 0.120 4 73451012 intron variant G/A;C snv 7
rs12304647
MIR196A2 ; HOXC6
0.807 0.160 12 53991163 intron variant A/C snv 0.26 6
rs9288516
XRCC5
0.827 0.120 2 216188541 intron variant T/A snv 5.0E-02 6
rs10932029
ICOS ; LOC101927840
0.827 0.200 2 203937045 intron variant T/A;C snv 5
rs28381975
PDCD6IP ; LOC105377023
0.827 0.200 3 33798239 intron variant -/TTACGTACCTGTGCA;TTCCGTACCTGTGCA;TTTCGTACCTGTGCA delins 5
rs3131034
DDR1
0.925 0.080 6 30886019 intron variant G/A snv 0.75 5
rs9268645
HLA-DRA
0.827 0.360 6 32440750 intron variant C/G;T snv 5
rs9277378
HLA-DPB1 ; HLA-DPA1
0.827 0.320 6 33082502 intron variant A/G snv 0.40 5
rs10272859
CDK14
0.925 0.120 7 90689160 intron variant G/C snv 0.39 4