Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs747432300 0.925 0.120 8 144504357 missense variant C/A;T snv 8.1E-06; 1.2E-04 2
rs1358379 0.882 0.160 6 71403739 intron variant T/C snv 6.2E-02 3
rs3820998 0.882 0.120 2 161138615 intron variant C/A;T snv 3
rs7536540 0.882 0.160 1 65058899 intron variant C/G;T snv 0.65 3
rs4656942 0.851 0.160 1 160861258 intron variant G/A;C;T snv 4
rs485618 0.851 0.160 1 160830690 3 prime UTR variant T/A;C;G snv 0.54 4
rs1054690270 0.827 0.160 8 144505907 frameshift variant CT/- delins 5
rs10932029 0.827 0.200 2 203937045 intron variant T/A;C snv 5
rs2233682 0.827 0.240 19 9838476 synonymous variant G/A snv 3.7E-02 6.3E-02 5
rs3129859 0.827 0.320 6 32433162 intergenic variant G/C;T snv 5
rs705382 0.827 0.200 7 95325909 upstream gene variant C/G snv 0.53 5
rs11003123 0.827 0.200 10 52771774 upstream gene variant G/A snv 0.30 6
rs12304647 0.807 0.160 12 53991163 intron variant A/C snv 0.26 6
rs2234671 0.807 0.240 2 218164385 missense variant C/G snv 9.1E-02 0.11 7
rs430397 0.763 0.240 9 125238840 intron variant C/T snv 9.1E-02 0.11 9
rs2896019 0.790 0.160 22 43937814 intron variant T/G snv 0.20 10
rs510432 0.752 0.280 6 106326155 upstream gene variant T/C snv 0.57 11
rs548234 0.763 0.360 6 106120159 intron variant C/T snv 0.76 11
rs13347 0.763 0.320 11 35231725 3 prime UTR variant C/A;T snv 12
rs9514828 0.752 0.440 13 108269025 intron variant C/T snv 0.35 12
rs2296651 0.732 0.240 14 69778476 missense variant G/A snv 6.3E-03 2.5E-03 13
rs5744174 0.742 0.360 1 223111186 missense variant A/G snv 0.39 0.34 13
rs2241883 0.763 0.360 2 88124547 missense variant T/C snv 0.30 0.29 14
rs3775290 0.742 0.280 4 186083063 missense variant C/A;T snv 0.30 15
rs3077 0.701 0.440 6 33065245 3 prime UTR variant A/G snv 0.29 16