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 3
rs10758669 0.763 0.280 9 4981602 upstream gene variant C/A;T snv 5
rs10806425 0.851 0.280 6 90216893 intron variant C/A snv 0.33 5
rs10903122 0.882 0.200 1 24977085 intergenic variant A/G snv 0.56 5
rs10995271 0.776 0.280 10 62678726 downstream gene variant G/C snv 0.32 3
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 4
rs11221332 0.763 0.280 11 128511079 intron variant C/A;T snv 5
rs11465804 0.752 0.320 1 67236843 intron variant T/G snv 4.4E-02 5.4E-02 3
rs11584383 0.827 0.200 1 200966738 downstream gene variant T/C snv 0.24 4
rs11712165 0.882 0.200 3 119399949 intron variant T/G snv 0.30 5
rs11747270 0.790 0.240 5 150879305 intron variant A/G snv 0.21 3
rs1250552 0.882 0.200 10 79298270 intron variant A/C;G snv 5
rs12928822 0.882 0.200 16 11310036 intron variant C/T snv 0.13 5
rs13003464 0.827 0.200 2 60959694 intron variant A/G snv 0.50 7
rs13010713 0.882 0.200 2 181131318 intron variant A/C;G snv 5
rs13098911 0.882 0.200 3 46193709 intron variant C/G;T snv 5
rs13151961 0.827 0.200 4 122194347 intron variant A/G snv 0.11 5
rs13314993 0.882 0.200 3 32973977 regulatory region variant G/C;T snv 5
rs1456893 0.851 0.160 7 50230076 intron variant G/A snv 0.69 3
rs1464510
LPP
0.807 0.280 3 188394766 intron variant C/A;T snv 7
rs1551398 0.882 0.160 8 125527809 intron variant G/A snv 0.48 3
rs17035378 0.882 0.200 2 68371823 intron variant T/A;C snv 5
rs1736135 0.851 0.160 21 15432901 intron variant T/C snv 0.33 4
rs1738074 0.790 0.320 6 159044945 5 prime UTR variant T/C snv 0.49 5