Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799963
F2
0.695 0.400 11 46739505 3 prime UTR variant G/A snv 9.6E-03 25
rs4906902 0.724 0.200 15 26774621 intron variant A/G snv 0.15 14
rs1046276 1.000 0.040 16 30903305 3 prime UTR variant T/C snv 0.62 3
rs10496964 0.925 0.040 2 144602342 intergenic variant C/T snv 0.12 2
rs12059546 0.925 0.040 1 239806797 intron variant A/G snv 0.30 2
rs121434579 0.925 0.040 5 161895774 missense variant C/A snv 2
rs763616736 0.925 0.080 17 50576111 missense variant C/T snv 2
rs2029461 1.000 0.040 6 34138013 intron variant C/T snv 0.43 1
rs3918149 1.000 0.040 6 32968596 5 prime UTR variant G/A snv 0.11 1
rs527539103 1.000 0.040 6 52479703 missense variant A/G snv 1
rs767833659 1.000 0.040 6 52465042 missense variant A/G snv 4.0E-06 1
rs779322943 1.000 0.040 6 52479211 missense variant T/C snv 4.0E-06 1
rs745600475 1.000 0.040 6 52438476 missense variant G/A;T snv 1.2E-05; 4.0E-06 1
rs543160745 1.000 0.040 6 52424148 missense variant A/G snv 4.0E-06; 7.6E-05 1
rs772265107 1.000 0.040 6 52490165 missense variant G/A;T snv 4.8E-05; 4.0E-06 1
rs1376122529 1.000 0.040 2 238252912 splice region variant G/A snv 4.0E-06 7.0E-06 1
rs1805032 1.000 0.040 2 151839238 stop gained G/A snv 4.0E-06 7.0E-06 3
rs79761183 0.925 0.040 6 52452776 missense variant G/A;C snv 2.0E-03; 8.0E-06; 1.2E-05 7.6E-03 2
rs772145901 1.000 0.040 19 603647 missense variant G/A;C snv 1.6E-05; 8.0E-06 1
rs764096785 1.000 0.040 6 52438370 missense variant C/T snv 1.2E-05 3.5E-05 1
rs534797617 1.000 0.040 6 52479212 missense variant A/C;G snv 1.6E-05 1
rs137852778 1.000 0.040 6 52454128 missense variant G/A;T snv 2.0E-05 1
rs765078446 0.925 0.040 6 53013900 missense variant T/G snv 2.0E-05 2.1E-05 3
rs780571007 1.000 0.040 6 52454113 missense variant A/G snv 3.2E-05 5.6E-05 1
rs149998588 1.000 0.040 6 52479759 stop gained C/T snv 3.2E-05 1.4E-05 1