Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1131691014
TP53
0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs61764370
KRAS
0.662 0.320 12 25207290 3 prime UTR variant A/C snv 6.2E-02 29
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs3746444
MIR499A ; MIR499B ; MYH7B ; LOC107985393
0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs1800469
B9D2 ; TGFB1
0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs2274223
PLCE1
0.620 0.400 10 94306584 missense variant A/G snv 0.28 0.31 40
rs4444903
EGF
0.630 0.360 4 109912954 5 prime UTR variant A/G snv 0.51 35
rs1169803481
EGFR
0.807 0.160 7 55198851 missense variant A/G snv 4.0E-06 7
rs779162432
PPIG
0.790 0.080 2 169637315 missense variant A/G snv 4.1E-06 7
rs4078289
DCC
1.000 0.080 18 53020735 intron variant A/G snv 0.75 1
rs121913279
PIK3CA
0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 101
rs5275
PTGS2
0.583 0.560 1 186673926 3 prime UTR variant A/G;T snv 55
rs1136201
ERBB2
0.645 0.280 17 39723335 missense variant A/G;T snv 0.20 34
rs743572
CYP17A1
0.672 0.360 10 102837395 5 prime UTR variant A/G;T snv 0.40; 8.1E-06 24
rs3824260
CYP7A1
0.742 0.160 8 58500631 upstream gene variant A/G;T snv 11
rs1800855
CCKAR
0.925 0.120 4 26489495 intron variant A/G;T snv 0.27 2
rs3834129
CASP8
0.627 0.560 2 201232809 upstream gene variant AGTAAG/- del 0.48 38
rs4940234
DCC
1.000 0.080 18 53012182 intron variant C/A snv 0.72 1
rs7504750
DCC
1.000 0.080 18 53021270 intron variant C/A snv 0.73 1
rs9944713
DCC
1.000 0.080 18 53008042 intron variant C/A snv 0.72 1
rs28934571
TP53
0.645 0.360 17 7674216 missense variant C/A;G snv 31
rs2303426
MSH2
0.790 0.080 2 47403411 intron variant C/A;G;T snv 1.9E-05; 0.47 8
rs4148217
ABCG8
0.790 0.280 2 43872294 missense variant C/A;T snv 0.21; 1.2E-05 11
rs2910164
MIR3142HG ; MIR146A
0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs1052133
OGG1 ; CAMK1
0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147