Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1223438908 1.000 0.120 3 105681480 missense variant T/G snv 4.0E-06 2
rs140101069 1.000 0.120 9 3828342 missense variant G/A snv 3.2E-04 8.4E-05 2
rs45450798 1.000 0.120 18 12792941 3 prime UTR variant C/G snv 0.12 2
rs752455542 1.000 0.120 3 105681740 missense variant T/G snv 4.0E-06 2
rs147846074 0.925 0.200 21 44289743 missense variant C/G;T snv 1.2E-05; 3.2E-05; 4.0E-06 3
rs4622308 0.925 0.160 12 56075401 upstream gene variant C/T snv 3
rs10272724 0.882 0.200 7 50409515 downstream gene variant T/C snv 0.24 4
rs1190356035 0.882 0.360 2 170853979 missense variant G/A snv 7.0E-06 4
rs1801208 0.882 0.360 4 6301162 missense variant G/A snv 5.7E-02 5.0E-02 4
rs2281808 0.925 0.160 20 1629905 intron variant T/A;C snv 4
rs1131017 0.925 0.160 12 56042145 5 prime UTR variant C/A;G;T snv 8.0E-06; 8.0E-06; 0.62; 1.1E-04 5
rs745826707 0.851 0.200 2 178112712 missense variant G/A;T snv 8.0E-06; 4.0E-06 5
rs229541 0.807 0.200 22 37195278 intron variant G/A snv 0.49 8
rs41295061 0.790 0.360 10 6072697 upstream gene variant C/A snv 6.1E-02 8
rs11203203 0.807 0.240 21 42416077 intron variant G/A snv 0.28 9
rs11594656 0.776 0.240 10 6080046 intergenic variant T/A snv 0.18 9
rs1678542 0.790 0.320 12 57574932 intron variant C/G snv 0.42 9
rs1738074 0.790 0.320 6 159044945 5 prime UTR variant T/C snv 0.49 9
rs3789604 0.776 0.360 1 113812320 synonymous variant T/A;C;G snv 8.5E-06; 1.3E-05; 0.17 9
rs2327832 0.790 0.320 6 137651931 intergenic variant A/G snv 0.16 10
rs3130544 0.807 0.360 6 31090563 intergenic variant C/A snv 7.4E-02 10
rs2488457 0.763 0.480 1 113872746 intron variant G/A;C snv 11
rs907715 0.752 0.520 4 122613898 intron variant C/T snv 0.35 11
rs12720356 0.752 0.360 19 10359299 missense variant A/C;G snv 6.1E-02; 4.0E-06 12
rs3733197 0.742 0.320 4 101918130 missense variant G/A snv 0.31 0.30 13