Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1276519904 0.645 0.520 1 226071445 missense variant A/G snv 63
rs1557644984 0.925 0.080 1 42927622 missense variant A/G snv 5
rs587776935 0.827 0.120 1 243505296 missense variant G/A snv 7
rs587779766 0.851 0.200 1 27549742 frameshift variant CA/- delins 7
rs587779767 0.851 0.200 1 27549218 frameshift variant G/- delins 7
rs587779768 0.851 0.200 1 27549569 frameshift variant G/- delins 7
rs61751035 0.882 0.160 1 213242186 missense variant G/A snv 2.4E-05 1.4E-05 6
rs730882203 0.851 0.080 1 46510953 missense variant C/T snv 6
rs752746786 0.742 0.560 1 1806503 missense variant A/C;G;T snv 4.0E-06 30
rs758432471 0.925 1 1806513 missense variant C/T snv 7.0E-06 4
rs869312821 0.882 0.120 1 1806515 missense variant T/C snv 7
rs869312822 0.827 0.200 1 1806514 missense variant A/C snv 8
rs869312823 0.882 0.080 1 1806509 missense variant T/C snv 9
rs869312824 0.827 0.200 1 1804565 missense variant A/G snv 14
rs869312825 0.827 0.120 1 1804548 start lost T/C snv 11
rs869312826 0.882 0.080 1 1787378 missense variant C/T snv 6
rs559979281 0.742 0.440 2 121530892 non coding transcript exon variant C/G;T snv 7.7E-06; 2.3E-05; 3.5E-04 23
rs863225422 0.742 0.440 2 121530927 non coding transcript exon variant G/A snv 4.6E-05; 7.7E-06 4.9E-05 23
rs1114167292 0.882 0.080 3 197704686 missense variant C/T snv 1.4E-05 6
rs1114167298 0.882 0.120 3 6861849 missense variant T/C snv 7.0E-06 5
rs1114167300 0.925 0.040 3 7578878 missense variant C/T snv 6
rs1114167301 0.925 0.040 3 7578930 missense variant C/A;T snv 4.0E-06 6
rs1559759089 0.827 0.200 3 113795101 missense variant C/A snv 14
rs1560212751 1.000 3 51208772 splice acceptor variant A/G snv 2
rs1560414254 1.000 3 51312486 frameshift variant ACTT/- delins 2