Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121912651 0.605 0.680 17 7674221 missense variant G/A;C snv 4.0E-06 53
rs121913343 0.611 0.520 17 7673803 missense variant G/A;C;T snv 1.2E-05 44
rs121912666 0.645 0.360 17 7674872 missense variant T/C;G snv 8.0E-06 34
rs1131691021 0.716 0.120 17 7675097 missense variant A/C;G snv 21
rs12947788 0.776 0.280 17 7674109 intron variant G/A snv 0.10 8
rs1555525012 0.882 0.200 17 7673603 missense variant G/A snv 3
rs17884306 0.925 0.120 17 7668783 3 prime UTR variant C/T snv 5.1E-02 2
rs78417682 0.925 0.120 7 47449305 intron variant G/C snv 0.15 2
rs2075685 0.724 0.320 5 83076846 intron variant G/A;T snv 14
rs3749474 0.724 0.320 4 55434518 3 prime UTR variant C/T snv 0.33 17
rs11943456 0.708 0.320 4 55410167 intron variant T/C snv 0.42 18
rs4927850 0.925 0.120 3 196024759 intron variant T/C snv 0.71 2
rs2736100 0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 83
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs5768709 0.925 0.120 22 48533757 intron variant A/G snv 0.36 2
rs2001389 0.925 0.120 10 102615501 intron variant G/A;C snv 3
rs1053004 0.776 0.280 17 42314074 3 prime UTR variant G/A snv 0.48 11
rs1053005 0.763 0.360 17 42313892 3 prime UTR variant T/C snv 0.25 10
rs4988487 0.925 0.120 16 1079193 missense variant C/A;T snv 4.0E-06; 5.3E-02 2
rs169068 0.742 0.280 16 1079872 missense variant C/T snv 0.54 0.50 12
rs4988483 0.752 0.240 16 1079010 missense variant C/A snv 3.7E-02 3.7E-02 11
rs17107315 0.620 0.440 5 147828115 missense variant T/C snv 9.1E-03 8.2E-03 40
rs111966833 0.776 0.320 5 147828053 missense variant G/A;C snv 4.5E-03 8
rs1799895 0.683 0.360 4 24800212 missense variant C/G snv 2.3E-02 1.2E-02 26
rs887303970 0.776 0.280 4 24799565 missense variant C/T snv 8.8E-06 7.0E-06 10