Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800449
LOX
0.641 0.400 5 122077513 missense variant C/A;T snv 4.0E-06; 0.17 33
rs4950928
CHI3L1
0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv 33
rs7799039
LOC105375494
0.649 0.560 7 128238730 upstream gene variant G/A;C snv 33
rs112445441
KRAS
0.658 0.400 12 25245347 missense variant C/A;G;T snv 32
rs760043106
TP53
0.645 0.440 17 7674947 missense variant A/C;G;T snv 32
rs121913227
BRAF
0.653 0.320 7 140753336 missense variant AC/CT;TT mnv 31
rs752021744
PIK3CB
0.689 0.440 3 138759306 missense variant T/C snv 1.2E-05 29
rs121913495
GNAS
0.672 0.400 20 58909366 missense variant G/A;T snv 28
rs1799977
MLH1
0.662 0.440 3 37012077 missense variant A/C;G;T snv 0.23 28
rs12785878
NADSYN1
0.677 0.520 11 71456403 intron variant G/A;T snv 25
rs4939827
SMAD7
0.708 0.160 18 48927093 intron variant T/A;C snv 25
rs876658657
MLH1
0.677 0.280 3 37020356 missense variant A/G snv 4.0E-06 25
rs1448674651
TYMS ; ENOSF1
0.667 0.560 18 671384 missense variant G/A;C snv 4.0E-06 23
rs1805097
IRS2
0.689 0.360 13 109782884 missense variant C/G;T snv 0.35 22
rs1039659576
MTR
0.689 0.520 1 236803473 missense variant A/G snv 21
rs9904341
BIRC5
0.695 0.280 17 78214286 5 prime UTR variant G/A;C;T snv 0.38; 4.8E-06 20
rs1042821
MSH6
0.732 0.280 2 47783349 missense variant G/A;C;T snv 0.18; 8.6E-06 16
rs7758229
SLC22A3
0.732 0.120 6 160419220 intron variant G/A;T snv 16
rs63750875
MSH2
0.742 0.280 2 47475171 missense variant G/A;C snv 1.6E-05 15
rs459552
APC
0.752 0.320 5 112841059 missense variant T/A;G snv 0.79 14
rs603965
CCND1
0.732 0.440 11 69648142 splice region variant G/A snv 14
rs750521832
MMP8
0.732 0.200 11 102718452 missense variant A/G snv 4.0E-06 14
rs12778366
SIRT1
0.724 0.480 10 67883321 upstream gene variant T/C;G snv 13
rs2228612
DNMT1
0.763 0.160 19 10162696 missense variant T/A;C;G snv 0.14 12
rs4987188
MSH2
0.790 0.200 2 47416318 missense variant G/A;T snv 1.3E-02; 2.0E-05 11