Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
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
rs211037 0.742 0.240 5 162101274 synonymous variant C/T snv 0.28 0.31 14
rs137852776 0.827 0.080 6 52452799 missense variant T/C snv 3.5E-03 2.4E-03 5
rs1805032 1.000 0.040 2 151839238 stop gained G/A snv 4.0E-06 7.0E-06 3
rs765078446 0.925 0.040 6 53013900 missense variant T/G snv 2.0E-05 2.1E-05 3
rs1046276 1.000 0.040 16 30903305 3 prime UTR variant T/C snv 0.62 3
rs1570624 0.882 0.040 6 52454252 missense variant G/A snv 1.0E-02 9.6E-03 3
rs121918817 0.882 0.040 2 166045080 missense variant C/T snv 1.7E-03 1.5E-03 3
rs10496964 0.925 0.040 2 144602342 intergenic variant C/T snv 0.12 2
rs763616736 0.925 0.080 17 50576111 missense variant C/T snv 2
rs12059546 0.925 0.040 1 239806797 intron variant A/G snv 0.30 2
rs149055334 0.925 0.040 6 52424111 missense variant C/A snv 1.9E-03 7.7E-03 2
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
rs121434579 0.925 0.040 5 161895774 missense variant C/A snv 2
rs3918149 1.000 0.040 6 32968596 5 prime UTR variant G/A snv 0.11 1
rs183899632 1.000 0.040 8 67746023 missense variant C/A;T snv 5.6E-05; 4.0E-05 1
rs137852777 1.000 0.040 6 52452742 missense variant G/A snv 4.8E-05 1
rs137852778 1.000 0.040 6 52454128 missense variant G/A;T snv 2.0E-05 1
rs142458862 1.000 0.040 6 52492274 missense variant T/G snv 1.8E-04 1.2E-04 1
rs149998588 1.000 0.040 6 52479759 stop gained C/T snv 3.2E-05 1.4E-05 1
rs17851770 1.000 0.040 6 52492273 missense variant A/C snv 6.2E-02 6.2E-02 1
rs200191497 1.000 0.040 6 52438562 missense variant C/T snv 7.2E-05 1.4E-05 1
rs371151471 1.000 0.040 6 52465092 missense variant C/T snv 1.2E-03 2.0E-04 1