Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1482518887
RUNX1
0.790 0.040 21 34887018 missense variant C/T snv 7.0E-06 8
rs869312828
DDX41 ; DOK3
0.807 0.080 5 177512369 missense variant C/T snv 7
rs1360131632
STAT5A
0.827 0.080 17 42301316 missense variant C/T snv 4.0E-06 6
rs2413739
PACSIN2
0.827 0.120 22 43001030 intron variant C/T snv 0.43 6
rs74315450
RUNX1
0.851 0.120 21 34859485 missense variant C/T snv 5
rs138817062
PML
0.882 0.040 15 74044940 missense variant C/T snv 4.0E-05 7.0E-06 4
rs35602083
FLT3
0.851 0.040 13 28049450 missense variant C/T snv 1.7E-02 1.6E-02 4
rs753000469
FLVCR1-DT ; FLVCR1
0.851 0.200 1 212859113 missense variant C/T snv 4.0E-06 4
rs754944509
CNTNAP1
0.851 0.080 17 42690793 missense variant C/T snv 4.4E-05 4
rs139834892
XRCC1
0.882 0.040 19 43553481 missense variant C/T snv 6.4E-05 1.1E-04 3
rs227060
C11orf65 ; ATM
0.882 0.160 11 108334154 intron variant C/T snv 0.27 3
rs1258094111
CTSG
0.925 0.040 14 24575388 missense variant C/T snv 4.0E-06 2
rs703817
STAT6
0.925 0.120 12 57096045 3 prime UTR variant C/T snv 0.39 2
rs754894156
RUNX1
0.925 0.040 21 34834544 missense variant C/T snv 4.0E-06 2
rs947141826
MTG1
0.925 0.040 10 133394281 missense variant C/T snv 2.1E-05 2
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1799782
XRCC1
0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs861539
KLC1 ; XRCC3
0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs1800566
NQO1
0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21 59
rs1979277
SHMT1
0.620 0.560 17 18328782 missense variant G/A snv 0.27 0.31 45
rs1275561861
HLA-A
0.672 0.360 6 29944350 missense variant G/A snv 23
rs174538
TMEM258 ; MIR611 ; FEN1
0.701 0.440 11 61792609 5 prime UTR variant G/A snv 0.34 0.26 21
rs2853677
TERT
0.724 0.240 5 1287079 3 prime UTR variant G/A snv 0.63 19
rs3807987
CAV1
0.732 0.280 7 116539780 intron variant G/A snv 7.6E-02 17