Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs985325188
APEX1 ; OSGEP
0.851 0.080 14 20456806 missense variant A/C snv 4
rs11016879
MGMT
0.882 0.040 10 129691518 intron variant A/C;G snv 0.66 4
rs7802034
XRCC2
0.925 0.040 7 152655183 intron variant A/C;G snv 2
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs786203436
TP53
0.701 0.280 17 7675125 missense variant A/C;G;T snv 20
rs4149570
TNFRSF1A
0.752 0.360 12 6342424 upstream gene variant A/C;G;T snv 11
rs1667255 0.925 0.040 18 31607316 intergenic variant A/C;G;T snv 3
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1695
GSTP1
0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs3746444
MIR499A ; MIR499B ; MYH7B ; LOC107985393
0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs2274223
PLCE1
0.620 0.400 10 94306584 missense variant A/G snv 0.28 0.31 40
rs2308321
MGMT
0.653 0.480 10 129766800 missense variant A/G snv 9.3E-02 8.7E-02 29
rs768623239
GSTM1 ; GSTM2
0.662 0.640 1 109689278 missense variant A/G snv 1.5E-05 26
rs1049253
CASP3
0.851 0.160 4 184627797 3 prime UTR variant A/G snv 0.13 4
rs11752942
LINC00951 ; TDRG1
0.882 0.080 6 40354019 intron variant A/G snv 0.46 3
rs1183646267
ATM
0.925 0.040 11 108281026 missense variant A/G snv 2
rs2234922
EPHX1
0.630 0.440 1 225838705 missense variant A/G;T snv 0.19; 2.8E-05 42
rs4553808
CTLA4
0.672 0.320 2 203866282 upstream gene variant A/G;T snv 0.16 28
rs747126003
IL6-AS1 ; IL6
0.689 0.400 7 22728790 missense variant A/G;T snv 4.0E-06 18
rs2014300
RUNX1
0.851 0.080 21 34985564 intron variant A/G;T snv 0.75 5
rs28362491
LOC105377621 ; NFKB1
0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 56
rs2736100
TERT
0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 83
rs3218373
XRCC2
0.827 0.120 7 152677078 upstream gene variant C/A snv 0.15 5
rs187238
IL18
0.602 0.680 11 112164265 intron variant C/A;G snv 48
rs764146326
TP53
0.662 0.480 17 7673779 missense variant C/A;G;T snv 4.0E-06 25