Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2070959 0.742 0.320 2 233693545 missense variant A/G snv 0.31 0.30 16
rs1051740 0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 56
rs1130864
CRP
0.672 0.520 1 159713301 3 prime UTR variant G/A snv 0.26 27
rs1800497 0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 56
rs11255841 0.776 0.080 10 8697617 intergenic variant T/A snv 0.25 11
rs10795668 0.724 0.160 10 8659256 upstream gene variant G/A snv 0.24 17
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs2855798 11 128863066 intron variant G/T snv 0.21 1
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs3842787 0.776 0.200 9 122371228 missense variant C/T snv 5.9E-02 8.5E-02 11
rs1799782 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs17503908 1.000 0.080 11 108344670 intron variant T/G snv 6.7E-02 2
rs2227999
XPC
3 14158408 missense variant C/T snv 4.2E-02 4.0E-02 1
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs5789 1.000 0.080 9 122381694 missense variant C/A snv 1.8E-02 1.8E-02 2
rs1201299 3 177053096 intron variant C/T snv 1.7E-02 1
rs61734277 0.882 0.080 6 10874672 missense variant A/C snv 9.1E-03 8.6E-03 5
rs1801166
APC
0.732 0.200 5 112839543 missense variant G/C snv 4.4E-03 5.6E-03 17
rs36053993 0.677 0.280 1 45331556 missense variant C/T snv 3.0E-03 3.3E-03 31
rs34612342 0.653 0.400 1 45332803 missense variant T/C snv 1.5E-03 1.6E-03 32
rs150766139 0.742 0.320 16 2046238 stop gained G/A snv 1.4E-03 1.4E-03 13
rs1801155
APC
0.649 0.440 5 112839514 missense variant T/A snv 8.0E-06; 2.0E-03 1.2E-03 42
rs142287570 1.000 6 10874335 missense variant T/G snv 6.6E-04 4.9E-04 2
rs142163070 8 142877100 missense variant T/C snv 2.0E-04 4.5E-04 1
rs55819519 0.627 0.400 17 7673751 missense variant C/A;G;T snv 1.6E-04 1.3E-04 40