Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4595552 0.790 0.080 11 125865825 intergenic variant C/G;T snv 7
rs1157
ALCAM
0.790 0.080 3 105576617 3 prime UTR variant G/A snv 0.16 7
rs13959
ALDH1A1
0.790 0.080 9 72930966 synonymous variant G/A snv 0.48 0.42 7
rs1444424830
FASTK
0.790 0.080 7 151078923 missense variant C/T snv 4.6E-06 7.0E-06 7
rs909629195
LASP1 ; MIR6779
0.790 0.080 17 38914448 missense variant C/T snv 7
rs951540403
PLCE1
0.790 0.080 10 94132433 missense variant G/C snv 7
rs779162432
PPIG
0.790 0.080 2 169637315 missense variant A/G snv 4.1E-06 7
rs775066324
TIMP2
0.790 0.080 17 78855710 missense variant G/A;C snv 4.0E-06; 4.0E-06 7
rs2303426
MSH2
0.790 0.080 2 47403411 intron variant C/A;G;T snv 1.9E-05; 0.47 8
rs35463555
NR1H2
0.776 0.160 19 50374423 intron variant G/A snv 0.29 8
rs4791171
AXIN2
0.763 0.080 17 65545379 intron variant T/C snv 0.55 11
rs2486758
CYP17A1
0.742 0.160 10 102837723 upstream gene variant T/C snv 0.18 11
rs3824260
CYP7A1
0.742 0.160 8 58500631 upstream gene variant A/G;T snv 11
rs6557634
TNFRSF10A
0.763 0.080 8 23202743 missense variant T/C snv 11
rs11954856
APC
0.732 0.200 5 112751630 intron variant T/G snv 0.54 12
rs1126497
EPCAM
0.716 0.200 2 47373967 missense variant T/C snv 0.51 0.58 14
rs2072668
OGG1
0.732 0.280 3 9756456 intron variant C/G snv 0.28 0.24 14
rs7922612
PLCE1
0.752 0.080 10 94051682 intron variant C/T snv 0.39 14
rs3808607
CYP7A1
0.716 0.400 8 58500365 upstream gene variant G/T snv 0.55 16
rs2695121
NR1H2
0.716 0.280 19 50377484 5 prime UTR variant T/C snv 0.70 16
rs7120118
NR1H3
0.716 0.360 11 47264739 intron variant T/C snv 0.38 18
rs743572
CYP17A1
0.672 0.360 10 102837395 5 prime UTR variant A/G;T snv 0.40; 8.1E-06 24
rs2250889
SLC12A5-AS1 ; MMP9
0.667 0.520 20 46013767 missense variant G/C;T snv 0.88; 1.6E-05 24
rs6259
SHBG
0.658 0.400 17 7633209 missense variant G/A snv 8.9E-02 8.1E-02 27
rs11887534
ABCG5 ; ABCG8
0.653 0.440 2 43839108 missense variant G/A;C snv 6.4E-06; 6.7E-02 29