Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9831894
CD86
0.882 0.120 3 122081640 intron variant A/C snv 0.31 3
rs931920092
EFS
0.925 0.120 14 23357350 missense variant G/A;C snv 2
rs909253
LTA ; LOC100287329
0.641 0.600 6 31572536 intron variant A/G;T snv 34
rs907715
IL21
0.752 0.520 4 122613898 intron variant C/T snv 0.35 11
rs895819
MIR23A ; LOC284454 ; MIR27A ; MIR24-2
0.623 0.560 19 13836478 non coding transcript exon variant T/A;C;G snv 0.34 0.38 46
rs879253942
TP53
0.677 0.400 17 7673826 missense variant A/G snv 28
rs8094402
MBP
0.882 0.120 18 76995493 intron variant A/G snv 0.25 3
rs806321
DLEU1
0.851 0.160 13 50267187 intron variant C/T snv 0.47 4
rs79480871 0.925 0.160 2 24471603 intergenic variant C/T snv 9.3E-02 2
rs79464052
ARAP3
1.000 0.120 5 141655607 intron variant G/C snv 7.1E-02 7.8E-02 1
rs777500092
DNMT3A
1.000 0.120 2 25246231 missense variant G/A snv 8.0E-06 2
rs7765004 0.925 0.120 6 113750518 regulatory region variant A/C snv 0.32 2
rs7712513
LOC101927357
0.925 0.120 5 122582513 intergenic variant G/T snv 0.71 2
rs770027749
XBP1
0.925 0.120 22 28795623 missense variant C/A;G snv 8.0E-06 2
rs764562217
TP53
0.882 0.120 17 7673308 stop lost T/G snv 2.3E-05 3.5E-05 3
rs758653954
EFS
0.925 0.120 14 23357350 frameshift variant -/C delins 4.0E-06; 8.0E-06 2
rs751837
CDC42BPB
0.882 0.120 14 103018488 intron variant T/C snv 0.23 4
rs745738344
TNF
0.653 0.600 6 31576786 synonymous variant G/A snv 1.6E-05 1.4E-05 28
rs730882026
TP53
0.742 0.440 17 7674256 missense variant T/C;G snv 15
rs6773854
LOC105374265
1.000 0.120 3 187931631 downstream gene variant T/C snv 0.23 2
rs6773363 1.000 0.120 3 27752141 intergenic variant T/A;C snv 1
rs6457327 0.790 0.320 6 31106253 downstream gene variant A/C snv 0.66 7
rs6449182
CD38
0.807 0.160 4 15778830 intron variant C/G snv 0.22 6
rs587781386
TP53
0.882 0.120 17 7674889 missense variant A/C;G snv 3.2E-05; 4.0E-06 3
rs587780073
TP53
0.708 0.400 17 7674262 missense variant T/C;G snv 19