Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10505477 0.658 0.400 8 127395198 intron variant A/G snv 0.40 31
rs10511729 0.742 0.240 9 23557229 intron variant T/G snv 0.35 11
rs11134527 0.677 0.400 5 168768351 intron variant G/A snv 0.25 24
rs12255372 0.667 0.480 10 113049143 intron variant G/A;T snv 28
rs12683422 0.742 0.240 9 27969442 intron variant C/T snv 5.7E-02 11
rs1380576 0.763 0.240 1 204519150 intron variant G/C snv 0.57 10
rs1447295 0.658 0.400 8 127472793 intron variant A/C;T snv 29
rs1520220 0.807 0.280 12 102402744 intron variant G/C;T snv 0.76 9
rs1562430 0.807 0.160 8 127375606 intron variant T/C snv 0.41 6
rs17045754 0.790 0.280 2 54269620 intron variant G/A;C snv 7
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs184003 0.724 0.400 6 32182519 intron variant C/A snv 0.12 0.12 15
rs2070744 0.608 0.680 7 150992991 intron variant C/T snv 0.70 54
rs207454
XDH
0.851 0.120 2 31344766 intron variant T/G snv 0.11 0.16 4
rs2094258 0.701 0.280 13 102844409 intron variant C/T snv 0.18 20
rs2298881 0.653 0.400 19 45423658 intron variant C/A;T snv 25
rs2808668
XPA
0.851 0.120 9 97690153 intron variant C/G;T snv 7
rs353639 0.851 0.120 11 35162817 intron variant T/G snv 0.32 5
rs3807987 0.732 0.280 7 116539780 intron variant G/A snv 7.6E-02 17
rs4938723 0.574 0.680 11 111511840 intron variant T/C snv 0.32 60
rs505922
ABO
0.689 0.520 9 133273813 intron variant C/T snv 34
rs6713088 0.763 0.200 2 54118332 intron variant C/G snv 0.48 9
rs744154 0.763 0.280 16 13921224 intron variant G/C snv 0.23 11