Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs533450458 0.925 0.120 8 90042781 missense variant C/T snv 5.5E-04 7.7E-05 2
rs9989419 0.882 0.120 16 56951227 regulatory region variant A/G snv 0.55 11
rs11572103 0.851 0.120 10 95058349 missense variant T/A snv 1.6E-02 4.9E-02 4
rs1223493898 0.851 0.120 20 44406090 missense variant G/A;C snv 5
rs1408888 0.851 0.120 13 71854515 intron variant T/G snv 0.30 5
rs2518136 0.851 0.120 3 186620038 intron variant T/C snv 0.46 4
rs7212 0.851 0.120 1 145992816 3 prime UTR variant G/C snv 0.16 5
rs805296 0.851 0.120 6 31655116 intron variant T/A;C snv 4
rs10757283 0.827 0.120 9 22134173 intergenic variant C/A;T snv 0.45 6
rs12050217 0.827 0.160 14 96262416 intron variant A/G snv 0.21 6
rs3088442 0.827 0.120 6 160451620 3 prime UTR variant G/A snv 0.28 5
rs6700896 0.827 0.160 1 65624099 intron variant C/T snv 0.44 9
rs9289231 0.827 0.120 3 124055231 intergenic variant T/G snv 0.15 5
rs10911021 0.807 0.160 1 182112825 intron variant C/T snv 0.36 11
rs1282382243 0.807 0.120 13 50843630 missense variant G/A snv 8
rs17366743 0.807 0.280 3 186854300 missense variant T/C snv 2.2E-02 2.1E-02 7
rs5082 0.807 0.160 1 161223893 upstream gene variant G/A snv 0.68 8
rs775381348 0.807 0.160 14 35308023 missense variant G/T snv 8
rs9267551 0.807 0.160 6 31730180 5 prime UTR variant C/G;T snv 7
rs146292819 0.790 0.240 9 104794495 missense variant T/G snv 2.9E-04 3.8E-04 9
rs16933090 0.790 0.160 11 16434247 5 prime UTR variant C/T snv 0.12 7
rs1800775 0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06 18
rs2297508 0.790 0.240 17 17812003 synonymous variant C/G;T snv 0.50; 7.5E-05 8
rs3732581 0.790 0.120 3 183840614 missense variant C/G;T snv 0.46; 1.2E-05 9
rs6850 0.790 0.160 7 44796715 5 prime UTR variant A/G;T snv 0.26; 4.0E-06 9