Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1058172
CYP2D6 ; NDUFA6-DT
0.882 0.080 22 42127526 missense variant C/G;T snv 4.4E-06; 9.2E-02 4
rs2014300
RUNX1
0.851 0.080 21 34985564 intron variant A/G;T snv 0.75 5
rs3746444
MIR499A ; MIR499B ; MYH7B ; LOC107985393
0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs758272654
GNAS
0.611 0.680 20 58909201 synonymous variant T/C snv 4.0E-06 7.0E-06 50
rs2424913
DNMT3B
0.708 0.440 20 32786453 intron variant C/T snv 0.56 0.53 18
rs3213173
E2F1
0.776 0.120 20 33677440 missense variant C/T snv 1.2E-03 5.1E-03 8
rs3213176
E2F1
0.776 0.120 20 33676869 missense variant C/T snv 1.9E-02; 5.1E-06 1.8E-02 8
rs522962
PTGIS
0.925 0.040 20 49526825 intron variant T/C snv 0.61 2
rs6019902
PTGIS
0.925 0.040 20 49561676 intron variant G/A snv 0.21 2
rs6125671
PTGIS
0.925 0.040 20 49559061 intron variant C/T snv 0.24 2
rs927068
PTGIS
0.925 0.040 20 49561437 intron variant G/T snv 0.32 2
rs25487
XRCC1
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs1799782
XRCC1
0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs13181
KLC3 ; ERCC2
0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs25489
XRCC1
0.550 0.720 19 43552260 missense variant C/G;T snv 8.5E-06; 7.1E-02 78
rs1799793
ERCC2
0.557 0.640 19 45364001 missense variant C/A;T snv 7.1E-06; 0.29 72
rs759412116
ERCC2
0.581 0.640 19 45352210 missense variant C/G;T snv 4.0E-06; 6.0E-05 55
rs1667255 0.925 0.040 18 31607316 intergenic variant A/C;G;T snv 3
rs1979277
SHMT1
0.620 0.560 17 18328782 missense variant G/A snv 0.27 0.31 45
rs397516436
TP53
0.641 0.440 17 7674894 stop gained G/A;C snv 34
rs1057519991
TP53
0.662 0.440 17 7675076 missense variant T/A;C;G snv 4.0E-06 26
rs764146326
TP53
0.662 0.480 17 7673779 missense variant C/A;G;T snv 4.0E-06 25
rs786203436
TP53
0.701 0.280 17 7675125 missense variant A/C;G;T snv 20
rs2240308
AXIN2
0.701 0.360 17 65558473 missense variant G/A snv 0.47 0.39 18
rs876659477
TP53
0.882 0.040 17 7673730 missense variant T/C snv 3