Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 33
rs17321515 0.776 0.200 8 125474167 intron variant A/G snv 0.49 16
rs11613352 0.827 0.160 12 57398797 intron variant C/T snv 0.19 9
rs1333047 0.790 0.240 9 22124505 intron variant A/T snv 0.63 9
rs12526453 0.827 0.160 6 12927312 intron variant C/G snv 0.27 5
rs2048327 0.851 0.120 6 160442500 intron variant T/C snv 0.28 5
rs765696008 0.925 0.080 19 11113268 intron variant G/A;C snv 2.8E-05; 4.0E-06 4
rs12720762 0.925 0.080 2 21043787 intron variant C/G snv 4.8E-03 2
rs587776886 0.925 0.080 19 11120608 intron variant C/G;T snv 2
rs879254734 0.925 0.080 19 11110640 intron variant G/A snv 2
rs12710260 1.000 0.080 19 11110781 intron variant G/A;C snv 1.2E-05; 0.40 1
rs540073140 1.000 0.080 19 11110780 intron variant C/T snv 3.2E-05 2.8E-05 1
rs515135 0.807 0.160 2 21063185 intergenic variant T/C snv 0.73 9
rs2228671 0.790 0.160 19 11100236 stop gained C/A;G;T snv 1.6E-05; 8.9E-02 14
rs752596535 0.752 0.200 19 11105407 stop gained C/A;G;T snv 1.6E-05 14
rs121908029 0.763 0.200 19 11105588 stop gained G/A;C;T snv 1.6E-05; 1.6E-05; 8.1E-06 13
rs11547917 0.807 0.200 19 11107491 stop gained C/A;G;T snv 7
rs121909374 0.790 0.120 11 47342578 stop gained C/A;G snv 1.3E-05 7
rs368657165 0.827 0.080 19 11107436 stop gained G/A;T snv 4.0E-05 7
rs121908031 0.851 0.160 19 11120425 stop gained C/A;G snv 8.0E-06 6
rs138947766 0.851 0.080 19 11116883 stop gained G/A;C snv 8.0E-06 6
rs144172724 0.851 0.080 19 11102774 stop gained G/A;T snv 1.6E-05 6
rs267607213 0.851 0.160 19 11100286 stop gained G/A;T snv 6
rs879254977 0.827 0.120 19 11116168 stop gained -/GCTGGTGA delins 6
rs121908035 0.882 0.160 19 11105599 stop gained C/A;G snv 5