Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs876659675
TP53
0.807 0.280 17 7674199 missense variant A/C;G;T snv 8
rs1057520004
TP53
0.752 0.240 17 7674884 missense variant A/C;T snv 12
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
rs5498
ICAM4 ; ICAM1
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs1136410
PARP1
0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs11615
ERCC1
0.572 0.640 19 45420395 synonymous variant A/G snv 0.50 0.55 62
rs1057519983
TP53
0.724 0.360 17 7673797 missense variant A/G snv 16
rs1057519933
PIK3CA
0.790 0.240 3 179199156 missense variant A/G snv 11
rs1057519935
PIK3CA
0.790 0.240 3 179199157 missense variant A/G snv 11
rs1057519841
PIK3R1
0.925 0.120 5 68295269 missense variant A/G snv 5
rs1057519888
EGFR
0.925 0.080 7 55143386 missense variant A/G snv 3
rs121913279
PIK3CA
0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 101
rs2234922
EPHX1
0.630 0.440 1 225838705 missense variant A/G;T snv 0.19; 2.8E-05 42
rs4646903
CYP1A1
0.630 0.640 15 74719300 downstream gene variant A/G;T snv 0.18 36
rs1057519936
PIK3CA
0.776 0.200 3 179234284 missense variant A/G;T snv 11
rs397517132
EGFR
0.623 0.280 7 55191846 missense variant A/T snv 48
rs1057519903
H3-3A
0.683 0.080 1 226064434 missense variant A/T snv 28
rs1057519926
PIK3CA
0.776 0.200 3 179210293 missense variant A/T snv 10
rs1200941109
MYCN ; MYCNOS
0.882 0.040 2 15940679 frameshift variant C/-;CC delins 4
rs2736100
TERT
0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 83
rs2606345
CYP1A1
0.732 0.360 15 74724835 intron variant C/A snv 0.46 16
rs762584624
MYL2
12 110919162 missense variant C/A snv 4.0E-06 1
rs121913286
PIK3CA
0.677 0.280 3 179218306 missense variant C/A;G snv 23
rs866775781
TP53
0.716 0.440 17 7675216 splice acceptor variant C/A;G snv 17