Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10045431 0.851 0.240 5 159387525 intron variant A/C snv 0.78 4
rs1063355 0.827 0.320 6 32659937 3 prime UTR variant T/G snv 0.56 5
rs10758669 0.763 0.280 9 4981602 upstream gene variant C/A;T snv 10
rs10995271 0.776 0.280 10 62678726 downstream gene variant G/C snv 0.32 8
rs11167764 0.925 0.120 5 142099500 regulatory region variant A/C snv 0.80 2
rs11175593 0.882 0.160 12 40208138 non coding transcript exon variant C/T snv 2.8E-02 3
rs11190140 0.827 0.160 10 99531836 upstream gene variant T/C snv 0.55 6
rs11209026 0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 46
rs11221332 0.763 0.280 11 128511079 intron variant C/A;T snv 13
rs11236797 0.790 0.200 11 76588605 upstream gene variant C/A snv 0.39 8
rs11465804 0.752 0.320 1 67236843 intron variant T/G snv 4.4E-02 5.4E-02 10
rs11584383 0.827 0.200 1 200966738 downstream gene variant T/C snv 0.24 5
rs11614913 0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs11747270 0.790 0.240 5 150879305 intron variant A/G snv 0.21 7
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs12232497 0.701 0.360 17 39883866 intergenic variant T/C snv 0.35 18
rs13003464 0.827 0.200 2 60959694 intron variant A/G snv 0.50 7
rs1456893 0.851 0.160 7 50230076 intron variant G/A snv 0.69 4
rs1551398 0.882 0.160 8 125527809 intron variant G/A snv 0.48 3
rs16969968 0.653 0.360 15 78590583 missense variant G/A snv 0.26 0.24 37
rs17235409 0.653 0.600 2 218395009 missense variant G/A;C snv 4.9E-02; 4.1E-06 31
rs17293632 0.763 0.240 15 67150258 intron variant C/T snv 0.17 12
rs1736135 0.851 0.160 21 15432901 intron variant T/C snv 0.33 4
rs174535 0.776 0.280 11 61783884 missense variant T/A;C;G snv 0.38 0.32 19
rs17582416 0.882 0.160 10 34998722 regulatory region variant T/G snv 0.31 3