Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs121909629
FGFR1
0.882 0.200 8 38415905 missense variant C/T snv 3
rs121912438
SOD1
0.605 0.520 21 31667299 missense variant G/A;C;T snv 1.2E-05; 8.0E-06 58
rs121913227
BRAF
0.653 0.320 7 140753336 missense variant AC/CT;TT mnv 31
rs121913237
NRAS
0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-06 50
rs121913250
NRAS
0.683 0.440 1 114716127 missense variant C/A;G;T snv 25
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs121913448
ABL1
0.827 0.120 9 130862976 missense variant G/A snv 5
rs121913452
ABL1
0.851 0.080 9 130873027 missense variant T/A;C;G snv 4
rs121913459
ABL1
0.672 0.160 9 130872896 missense variant C/T snv 25
rs121913461
ABL1
0.851 0.120 9 130862970 missense variant T/C snv 5
rs121913488
FLT3
0.807 0.120 13 28018505 missense variant C/A;G;T snv 7
rs121913502
IDH2
0.708 0.320 15 90088702 missense variant C/A;T snv 3.2E-05 19
rs121913507
KIT
0.614 0.400 4 54733155 missense variant A/T snv 49
rs121913514
KIT
0.763 0.240 4 54733174 missense variant T/A;G snv 12
rs121913521
KIT
0.790 0.120 4 54727447 missense variant T/A;C;G snv 12
rs121913529
KRAS
0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 144
rs121913615
MPL
0.683 0.240 1 43349338 missense variant G/C;T snv 8.0E-06 25
rs121913682
KIT
0.605 0.400 4 54733167 missense variant A/G;T snv 52
rs121918464
PTPN11
0.708 0.440 12 112450406 missense variant G/A;C snv 25
rs1258094111
CTSG
0.925 0.040 14 24575388 missense variant C/T snv 4.0E-06 2
rs1275561861
HLA-A
0.672 0.360 6 29944350 missense variant G/A snv 23
rs13181
KLC3 ; ERCC2
0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs1360131632
STAT5A
0.827 0.080 17 42301316 missense variant C/T snv 4.0E-06 6
rs1360698171
RNASEL
0.851 0.080 1 182584103 missense variant T/C snv 4