Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 59
rs10896449 0.827 0.200 11 69227200 intergenic variant A/G snv 0.53 6
rs12826786 0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38 26
rs2410373 0.851 0.120 8 16066997 intergenic variant A/C snv 0.34 6
rs2660753 0.790 0.240 3 87061524 intergenic variant T/C snv 0.76 8
rs406193 0.882 0.120 20 32811837 downstream gene variant T/C snv 0.91 5
rs6983269 0.925 0.080 8 2741967 intron variant C/A;G;T snv 0.42 4
rs9325782 0.851 0.120 8 16232964 intron variant C/T snv 0.87 6
rs9600079 0.925 0.080 13 73154002 intergenic variant G/T snv 0.46 5
rs2231142 0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 54
rs505922
ABO
0.689 0.520 9 133273813 intron variant C/T snv 20
rs266729 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs822395 0.776 0.240 3 186849018 intron variant C/A;G snv 10
rs822396 0.732 0.400 3 186849088 intron variant G/A snv 0.81 16
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs2241766 0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13 48
rs12529 0.776 0.280 10 5094459 missense variant C/G snv 0.50 0.45 10
rs121434592 0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 54
rs7254617 0.882 0.120 19 40285605 upstream gene variant G/A;C;T snv 5
rs1463038513
APC
0.658 0.440 5 112839511 frameshift variant TAAA/- delins 36
rs1801155
APC
0.649 0.440 5 112839514 missense variant T/A snv 8.0E-06; 2.0E-03 1.2E-03 36
rs1130409 0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 72
rs137852593
AR
0.827 0.160 X 67717484 missense variant G/A;C;T snv 2.2E-05; 1.1E-05; 9.1E-04 7
rs34301344 0.689 0.400 13 49630893 stop gained G/A snv 9.7E-03 7.9E-03 22
rs3803185 0.708 0.320 13 49630889 missense variant T/C;G snv 0.39 19