Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11167764 0.925 0.120 5 142099500 regulatory region variant A/C snv 0.80 2
rs199883290 0.925 0.120 16 50729867 missense variant G/A;C snv 4.0E-06; 1.5E-02 7.0E-06 2
rs224136 0.925 0.120 10 62710915 intron variant C/A;T snv 0.34 2
rs540973741 0.925 0.120 16 50729868 frameshift variant C/-;CC delins 2
rs76181804 0.925 0.120 1 198632575 intergenic variant A/G snv 8.2E-02 2
rs11175593 0.882 0.160 12 40208138 non coding transcript exon variant C/T snv 2.8E-02 3
rs1551398 0.882 0.160 8 125527809 intron variant G/A snv 0.48 3
rs17582416 0.882 0.160 10 34998722 regulatory region variant T/G snv 0.31 3
rs3135499 0.882 0.160 16 50732216 splice donor variant A/C snv 0.45 3
rs3828309 0.882 0.160 2 233271764 intron variant A/G snv 0.42 3
rs10045431 0.851 0.240 5 159387525 intron variant A/C snv 0.78 4
rs1456893 0.851 0.160 7 50230076 intron variant G/A snv 0.69 4
rs1736135 0.851 0.160 21 15432901 intron variant T/C snv 0.33 4
rs4613763 0.851 0.240 5 40392626 regulatory region variant T/C snv 0.14 4
rs762421 0.851 0.360 21 44195678 intron variant G/A snv 4
rs9286879 0.851 0.200 1 172893094 intron variant A/G snv 0.32 4
rs1063355 0.827 0.320 6 32659937 3 prime UTR variant T/G snv 0.56 5
rs11584383 0.827 0.200 1 200966738 downstream gene variant T/C snv 0.24 5
rs2188962 0.882 0.160 5 132435113 intron variant C/T snv 0.29 5
rs3135500 0.851 0.160 16 50732975 3 prime UTR variant G/A snv 0.44 5
rs6927172 0.851 0.120 6 137681038 intron variant C/A;G;T snv 5
rs7746082 0.851 0.160 6 105987394 regulatory region variant G/A;C snv 5
rs8005161 0.882 0.120 14 88006251 intron variant C/T snv 0.18 5
rs11190140 0.827 0.160 10 99531836 upstream gene variant T/C snv 0.55 6
rs2274910 0.827 0.200 1 160882256 non coding transcript exon variant T/C snv 0.65 0.58 6