Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs149127230 1.000 0.080 16 68823566 stop gained G/A;C;T snv 1.7E-04; 4.0E-06 1
rs35572355 1.000 0.080 16 68833344 missense variant G/A;C snv 1.7E-04; 4.0E-06 1
rs587776398 1.000 0.080 16 68812149 stop gained T/C;G snv 3.6E-05 1
rs587780784 1.000 0.080 16 68811854 stop gained C/G;T snv 1.6E-05; 8.0E-06 2
rs121964873 0.925 0.080 16 68810290 stop gained G/A;T snv 1.2E-05 2
rs1060501244 1.000 0.080 16 68828204 missense variant G/A;T snv 8.0E-06 2
rs876659503 1.000 0.080 16 68810302 stop gained G/A;C;T snv 8.0E-06 1
rs876659716 1.000 0.080 16 68819283 stop gained T/A;C snv 8.0E-06 2
rs771085839 1.000 0.080 16 68808692 splice acceptor variant G/C snv 4.0E-06 1
rs876661106 1.000 0.080 16 68801843 stop gained A/G;T snv 4.0E-06 1
rs971882211 1.000 0.080 16 68823404 stop gained G/C;T snv 4.0E-06 2.1E-05 1
rs121964874 1.000 0.080 16 68823557 stop gained C/A;G;T snv 4.0E-06 1
rs781409616 1.000 0.080 16 68801789 stop gained C/T snv 4.0E-06 1
rs1375617541 1.000 0.080 16 68829739 frameshift variant -/C delins 4.0E-06 1
rs876660771 1.000 0.080 16 68812264 splice donor variant G/A snv 4.0E-06 7.0E-06 2
rs587780787 1.000 0.080 16 68828296 stop gained G/T snv 4.0E-06 2
rs587782750 1.000 0.080 16 68822210 stop gained C/T snv 4.0E-06 2
rs746481984 0.851 0.120 16 68819393 missense variant C/G;T snv 4.0E-06 3
rs104894360 0.724 0.560 12 25209904 missense variant T/A;C snv 14
rs587782798 0.807 0.400 16 68813322 stop gained C/T snv 7
rs876658932 0.807 0.400 16 68801726 stop gained C/G;T snv 7
rs1555515731 0.882 0.160 16 68812189 frameshift variant T/- delins 4
rs587780537 0.925 0.080 16 68810224 missense variant G/A snv 3
rs876659384 0.851 0.240 17 7673552 stop gained C/A snv 3
rs1057517542 1.000 0.080 16 68829653 splice acceptor variant G/A snv 2