Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs77375493 0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 187
rs387907272 0.572 0.520 3 38141150 stop lost T/C snv 5.2E-05 7.0E-06 73
rs201478192 0.790 0.200 2 8731667 missense variant C/A snv 2.4E-04 2.6E-04 12
rs2071286 0.752 0.280 6 32212119 intron variant C/T snv 0.17 12
rs104893626 0.827 0.280 2 136114915 stop gained G/C snv 11
rs9461776 0.763 0.240 6 32607958 intergenic variant A/G snv 8.8E-02 11
rs1426488816 0.827 0.160 9 26913948 splice acceptor variant C/T snv 8.0E-06 9
rs773862672 0.882 0.280 1 11247922 missense variant G/A;C snv 1.2E-05 6
rs75002266 0.827 0.160 2 147939241 missense variant G/A snv 3.2E-03 3.0E-03 6
rs757085537 0.851 0.160 6 106105356 missense variant C/T snv 7.0E-06 5
rs1472503583 0.925 0.160 19 1360712 missense variant C/T snv 4.0E-06 4