Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs1042714 0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs56149945 0.595 0.680 5 143399752 missense variant T/A;C snv 2.0E-02 49
rs2241766 0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13 48
rs886041065 0.677 0.600 2 25743913 frameshift variant G/- delins 43
rs1232898090 0.637 0.600 22 46198429 missense variant G/C;T snv 4.0E-06; 4.0E-06 40
rs266729 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs1799883 0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 36
rs11575937 0.653 0.480 1 156136985 missense variant G/A;T snv 29
rs78311289 0.689 0.440 4 1806162 missense variant A/C;G snv 4.0E-06 25
rs13266634 0.724 0.480 8 117172544 missense variant C/A;T snv 0.29 23
rs1718119 0.689 0.520 12 121177300 missense variant G/A;T snv 0.35; 4.0E-06 21
rs80356814 0.732 0.320 1 156138697 synonymous variant C/T snv 8.0E-06 15
rs137852671 0.790 0.160 11 17394295 missense variant C/T snv 10
rs3732581 0.790 0.120 3 183840614 missense variant C/G;T snv 0.46; 1.2E-05 9
rs587777732 0.763 0.240 20 44406195 missense variant C/T snv 9
rs1057515572 0.882 0.200 7 5987033 frameshift variant GC/ACT delins 8
rs628031 0.807 0.280 6 160139813 missense variant A/C;G snv 5.3E-05; 0.63 8
rs121909731 0.851 0.120 10 87057692 missense variant G/A;C snv 4.0E-06 7
rs683369 0.807 0.360 6 160130172 missense variant G/A;C;T snv 4.0E-06; 0.83; 4.0E-06 7
rs146488435 0.851 0.080 17 63533914 missense variant C/G;T snv 8.0E-06; 6.4E-05 5
rs1057518775 0.851 0.160 11 17387907 missense variant G/A;C snv 4
rs121909730 0.882 0.040 10 87053380 missense variant G/A snv 4
rs2288377 0.925 0.080 12 102480984 intron variant A/G;T snv 2
rs587777260 0.925 0.080 13 75359852 stop gained G/A;T snv 4.0E-06 2