Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs4938723 0.574 0.680 11 111511840 intron variant T/C snv 0.32 60
rs2070744 0.608 0.680 7 150992991 intron variant C/T snv 0.70 54
rs1799750 0.592 0.760 11 102799765 intron variant C/- delins 0.50 48
rs2279744 0.605 0.640 12 68808800 intron variant T/G snv 0.31 48
rs243865 0.600 0.640 16 55477894 intron variant C/T snv 0.19 48
rs920778 0.633 0.480 12 53966448 intron variant G/A snv 0.57 36
rs505922
ABO
0.689 0.520 9 133273813 intron variant C/T snv 34
rs909253 0.641 0.600 6 31572536 intron variant A/G;T snv 34
rs10505477 0.658 0.400 8 127395198 intron variant A/G snv 0.40 31
rs1447295 0.658 0.400 8 127472793 intron variant A/C;T snv 29
rs12255372 0.667 0.480 10 113049143 intron variant G/A;T snv 28
rs1927911 0.658 0.640 9 117707776 intron variant A/G snv 0.62 28
rs11066280 0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 27
rs2298881 0.653 0.400 19 45423658 intron variant C/A;T snv 25
rs11134527 0.677 0.400 5 168768351 intron variant G/A snv 0.25 24
rs4778889 0.683 0.480 15 81296654 intron variant T/C snv 0.24 24
rs744166 0.689 0.560 17 42362183 intron variant A/G snv 0.48 22
rs2094258 0.701 0.280 13 102844409 intron variant C/T snv 0.18 20
rs7804372 0.716 0.320 7 116554174 intron variant T/A snv 0.27 19
rs2074356 0.763 0.280 12 112207597 intron variant G/A snv 3.8E-03 18
rs2424913 0.708 0.440 20 32786453 intron variant C/T snv 0.56 0.53 18