Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10505474 0.925 0.080 8 127405259 intron variant T/C snv 0.47 3
rs12757998 0.925 0.080 1 182569343 downstream gene variant C/T snv 0.24 3
rs1450063773 0.925 0.080 19 50858491 missense variant C/A;T snv 8.0E-06; 4.0E-06 3
rs16901966 0.925 0.080 8 127098007 intron variant A/G snv 0.13 3
rs1859962 0.882 0.160 17 71112612 intron variant G/T snv 0.56 3
rs266849 0.925 0.080 19 50845834 intron variant G/A snv 0.82 3
rs267605077 0.925 0.080 17 7675212 missense variant A/G;T snv 3
rs2707765
APC
0.925 0.080 5 112786835 intron variant G/A;C;T snv 3
rs3747531 0.925 0.080 8 16155139 missense variant G/A;C snv 3
rs41441651 0.925 0.080 6 32396111 missense variant C/T snv 2.3E-02 9.5E-03 3
rs6470517 0.925 0.080 8 127448159 intron variant A/G snv 0.15 3
rs1060501201 0.925 0.080 17 7674190 missense variant T/C;G snv 4
rs1197734477 0.925 0.080 10 87961012 missense variant A/G snv 4
rs137852581
AR
0.882 0.080 X 67723701 missense variant C/T snv 4
rs149709822 0.882 0.080 19 50856335 missense variant G/A snv 4.0E-05 2.3E-04 4
rs17632542 0.925 0.080 19 50858501 missense variant T/C snv 5.5E-02 4.9E-02 4
rs1902023 0.882 0.080 4 68670366 missense variant A/C snv 0.51 0.53 4
rs565453 0.882 0.160 5 112849696 intron variant A/C;G snv 4
rs822391 0.925 0.080 3 186846014 intron variant C/T snv 0.85 4
rs864622007
AR
0.882 0.200 X 67711621 missense variant T/A snv 4
rs1042489 0.851 0.160 17 78224125 3 prime UTR variant T/C snv 0.40 5
rs1290923018 0.851 0.160 11 65570699 missense variant G/A snv 4.0E-06 5
rs1512268 0.851 0.160 8 23668950 intergenic variant T/C snv 0.50 5
rs2735839 0.827 0.160 19 50861367 upstream gene variant A/C;G snv 5
rs3774262 0.851 0.200 3 186854025 intron variant G/A snv 0.10 5