Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057520015 1.000 0.080 18 20955181 missense variant G/A snv 2
rs1057519857 0.882 0.080 17 39724772 missense variant T/C snv 4
rs121913469 0.763 0.240 17 39723966 missense variant TT/CC mnv 11
rs587781991 0.724 0.240 17 7675208 missense variant C/A;T snv 17
rs1273593548 0.716 0.160 7 106867593 missense variant T/G snv 8.4E-06 19
rs121913348 0.763 0.480 7 140781617 missense variant C/A;G;T snv 20
rs483352697 0.695 0.480 17 7674944 missense variant C/A;G;T snv 4.0E-06 21
rs587781525 0.689 0.480 17 7673778 missense variant T/A;C;G snv 22
rs121913286 0.677 0.280 3 179218306 missense variant C/A;G snv 23
rs3803662 0.662 0.440 16 52552429 non coding transcript exon variant A/G snv 0.63 25
rs6505162 0.695 0.320 17 30117165 5 prime UTR variant A/C;T snv 0.50; 3.1E-05 25
rs1058808 0.658 0.360 17 39727784 missense variant C/G snv 0.61 0.52 27
rs760043106 0.645 0.440 17 7674947 missense variant A/C;G;T snv 32
rs886039484 0.641 0.440 17 7674888 missense variant T/C;G snv 32
rs1057519975 0.649 0.480 17 7675209 missense variant A/C;G;T snv 34
rs752742313 0.637 0.320 3 138655502 missense variant C/T snv 1.2E-05 36
rs121913233 0.627 0.520 11 533874 missense variant T/A;C;G snv 37
rs121913281 0.623 0.520 3 179234296 missense variant C/T snv 37
rs2273535 0.645 0.360 20 56386485 missense variant A/C;T snv 0.28 38
rs727503094 0.633 0.440 11 534287 missense variant GC/AG;AT;TA;TT mnv 41
rs17879961 0.597 0.480 22 28725099 missense variant A/C;G snv 4.1E-03 53
rs121434592 0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 54
rs11540652 0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 57
rs104886003 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 71
rs104894229 0.564 0.600 11 534289 missense variant C/A;G;T snv 73