Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9642393
EGFR
0.925 0.040 7 55177954 intron variant T/C snv 0.24 2
rs1259560536
ADAM33
1.000 0.040 20 3671756 missense variant T/C snv 7.0E-06 1
rs13181
KLC3 ; ERCC2
0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs121913444
EGFR
0.724 0.160 7 55191831 missense variant T/A;C;G snv 18
rs2243248
IL4
0.763 0.240 5 132672952 upstream gene variant T/A;C;G snv 9
rs10852606
HEATR3
0.882 0.040 16 50094961 intron variant T/A;C snv 4
rs1057519904
H3C11
0.742 0.080 6 27872233 missense variant T/A snv 17
rs17296479 0.851 0.040 5 81411157 non coding transcript exon variant T/A snv 9.4E-02 5
rs373191257
AMFR
0.827 0.080 16 56363027 missense variant T/A snv 1.6E-05 7.0E-06 5
rs2017309
CHEK2
0.851 0.040 22 28735438 intron variant T/A snv 0.23 4
rs572480837
POU5F1 ; TCF19
0.851 0.040 6 31165582 missense variant T/A snv 5.0E-04 8.4E-05 4
rs878854066
TP53
0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs3829382
FLT3
0.925 0.040 13 28003551 3 prime UTR variant G/T snv 0.46 2
rs8957
SLC2A4RG
0.925 0.040 20 63742354 missense variant G/T snv 0.71 0.78 2
rs1042522
TP53
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs11558961
GFAP
0.925 0.040 17 44907319 3 prime UTR variant G/C;T snv 0.27; 1.2E-05 2
rs1057519902
H3-3A
0.742 0.160 1 226064451 missense variant G/C snv 16
rs1801320
RAD51 ; RAD51-AS1
0.742 0.160 15 40695330 5 prime UTR variant G/C snv 0.12 15
rs660118
SART1
0.807 0.080 11 65967703 missense variant G/C snv 0.46 0.36 6
rs76151636
ATP7B
0.776 0.280 13 51944145 missense variant G/A;T snv 4.0E-06; 9.2E-04 10
rs745542298
TP73
0.807 0.080 1 3732781 missense variant G/A;T snv 8.6E-06; 4.3E-06 2.1E-05 6
rs374052197
PDPN
0.882 0.040 1 13610421 missense variant G/A;T snv 8.0E-06 5
rs774238794
HDAC9
0.925 0.080 7 18644690 missense variant G/A;T snv 4.1E-05; 4.1E-06 2
rs121912438
SOD1
0.605 0.520 21 31667299 missense variant G/A;C;T snv 1.2E-05; 8.0E-06 58
rs121913499
IDH1
0.605 0.520 2 208248389 missense variant G/A;C;T snv 51