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
rs11887534
ABCG5 ; ABCG8
0.653 0.440 2 43839108 missense variant G/A;C snv 6.4E-06; 6.7E-02 29
rs4148217
ABCG8
0.790 0.280 2 43872294 missense variant C/A;T snv 0.21; 1.2E-05 11
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
rs11954856
APC
0.732 0.200 5 112751630 intron variant T/G snv 0.54 12
rs693
APOB
0.708 0.440 2 21009323 synonymous variant G/A snv 0.39 0.38 24
rs4791171
AXIN2
0.763 0.080 17 65545379 intron variant T/C snv 0.55 11
rs1800469
B9D2 ; TGFB1
0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs3834129
CASP8
0.627 0.560 2 201232809 upstream gene variant AGTAAG/- del 0.48 38
rs1800855
CCKAR
0.925 0.120 4 26489495 intron variant A/G;T snv 0.27 2
rs2071011
CCKAR
1.000 0.080 4 26489811 intron variant C/G;T snv 1
rs3822222
CCKAR
1.000 0.080 4 26489030 intron variant G/A snv 0.14 1
rs915889
CCKAR
1.000 0.080 4 26484572 intron variant G/A snv 0.15 1
rs708272
CETP
0.708 0.440 16 56962376 intron variant G/A snv 0.42 0.38 24
rs975334
CNTN4
0.925 0.080 3 2804632 intron variant G/A snv 0.50 2
rs743572
CYP17A1
0.672 0.360 10 102837395 5 prime UTR variant A/G;T snv 0.40; 8.1E-06 24
rs2486758
CYP17A1
0.742 0.160 10 102837723 upstream gene variant T/C snv 0.18 11
rs1048943
CYP1A1
0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 88
rs3808607
CYP7A1
0.716 0.400 8 58500365 upstream gene variant G/T snv 0.55 16
rs3824260
CYP7A1
0.742 0.160 8 58500631 upstream gene variant A/G;T snv 11
rs7504990
DCC
0.851 0.120 18 52991406 intron variant T/C snv 0.73 4
rs4078288
DCC
0.882 0.120 18 53020881 intron variant G/A snv 0.73 3
rs11082960
DCC
1.000 0.080 18 52999470 intron variant G/T snv 0.72 1
rs4077283
DCC
1.000 0.080 18 53019949 intron variant G/A snv 0.72 1