Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs74315355 0.790 0.080 1 20644639 missense variant G/A snv 7
rs1060499619 0.851 0.040 21 32681590 missense variant C/G snv 4
rs137853055 1.000 0.040 6 161569357 stop gained G/A snv 1
rs137853056 1.000 0.040 6 161350139 stop gained C/T snv 1
rs137853057 1.000 0.040 6 162201182 missense variant T/A snv 1
rs1554391082 1.000 0.040 7 131556270 frameshift variant -/GGCGACGG delins 1
rs1562430103 1.000 0.040 6 161973301 splice donor variant C/T snv 1
rs1562485799 1.000 0.040 6 162054149 stop gained A/C snv 1
rs397514694 1.000 0.040 6 161350205 missense variant C/A snv 1
rs397518439 1.000 0.040 6 162727661 splice donor variant C/A;G snv 1
rs55961220 1.000 0.040 6 161785778 missense variant A/C snv 1
rs754809877 1.000 0.040 6 162443326 frameshift variant T/- delins 3.1E-04 1
rs137853054 0.882 0.160 6 161973317 missense variant G/A;C;T snv 3.7E-04; 4.0E-06; 8.0E-06 4
rs147757966 0.925 0.040 6 162443383 missense variant C/A;G;T snv 4.0E-06; 8.8E-05 2
rs9456735 1.000 0.040 6 162054135 start lost T/A;G snv 4.0E-06; 4.4E-03 1
rs532703934 1.000 0.040 6 162443438 missense variant C/A;T snv 4.0E-06; 4.0E-06 1
rs33939927 0.708 0.120 12 40310434 missense variant C/A;G;T snv 4.0E-06; 1.2E-05 24
rs2066842 0.763 0.200 16 50710713 missense variant C/A;T snv 4.0E-06; 0.19 15
rs778125254 1.000 0.040 6 161360129 missense variant G/T snv 8.0E-06 1
rs55774500 1.000 0.040 6 162262692 missense variant G/A;T snv 8.0E-06; 3.6E-03 1
rs34424986 0.752 0.200 6 161785820 missense variant G/A;T snv 1.9E-03; 8.0E-06 10
rs398122403 0.807 0.080 21 32695106 missense variant C/T snv 1.2E-05 11
rs137853058 0.882 0.120 6 161973401 missense variant C/T snv 1.2E-05 3
rs566229879 1.000 0.040 6 162262662 missense variant G/A snv 1.2E-05 1
rs751037529 0.925 0.040 6 161785793 missense variant C/G snv 1.2E-05 3