Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1183194405
F2
0.716 0.440 11 46719773 missense variant G/A;T snv 4.5E-06; 4.5E-06 19
rs35761398 0.701 0.520 1 23875429 missense variant TT/CC mnv 19
rs2501432 0.716 0.480 1 23875430 missense variant T/C;G snv 0.62 16
rs4246905 0.716 0.400 9 114790969 missense variant T/A;C snv 0.76 16
rs2066842 0.763 0.200 16 50710713 missense variant C/A;T snv 4.0E-06; 0.19 15
rs879761216 0.732 0.480 1 23875429 frameshift variant TT/C;T delins 14
rs11221332 0.763 0.280 11 128511079 intron variant C/A;T snv 13
rs12720356 0.752 0.360 19 10359299 missense variant A/C;G snv 6.1E-02; 4.0E-06 12
rs16910526 0.742 0.280 12 10118488 stop gained A/C;G snv 6.2E-02 12
rs2872507 0.752 0.360 17 39884510 intergenic variant G/A;T snv 12
rs3939286 0.776 0.360 9 6210099 regulatory region variant T/A;C snv 12
rs7530511 0.742 0.400 1 67219704 missense variant T/A;C snv 0.88 12
rs10748781 0.763 0.160 10 99523573 upstream gene variant C/A;G snv 11
rs4077515 0.763 0.360 9 136372044 missense variant C/A;T snv 4.0E-06; 0.41 11
rs4149570 0.752 0.360 12 6342424 upstream gene variant A/C;G;T snv 11
rs10758669 0.763 0.280 9 4981602 upstream gene variant C/A;T snv 10
rs4845604 0.776 0.200 1 151829204 intron variant G/A;C;T snv 10
rs1142345 0.776 0.280 6 18130687 missense variant T/C;G snv 3.7E-02 9
rs11230563 0.790 0.360 11 61008737 missense variant C/G;T snv 4.2E-06; 0.31 8
rs1248696 0.807 0.080 10 77856847 missense variant T/A;C snv 0.93 8
rs212388 0.827 0.240 6 159069404 intron variant C/G;T snv 8
rs235768 0.807 0.160 20 6778468 missense variant A/G;T snv 0.67 8
rs33972313 0.790 0.160 5 139379813 missense variant C/A;G;T snv 4.0E-06; 2.7E-02 8
rs12942547 0.807 0.200 17 42375526 intron variant A/G;T snv 7
rs13306190 0.807 0.320 2 21032408 missense variant G/A;C;T snv 1.7E-04; 8.0E-06 7