Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs7679673 | 0.677 | 0.440 | 4 | 105140377 | intron variant | C/A | snv | 0.50 | 25 | ||
rs121913286 | 0.677 | 0.280 | 3 | 179218306 | missense variant | C/A;G | snv | 22 | |||
rs7931342 | 0.689 | 0.360 | 11 | 69227030 | intergenic variant | T/G | snv | 0.58 | 19 | ||
rs10505477 | 0.658 | 0.400 | 8 | 127395198 | intron variant | A/G | snv | 0.40 | 13 | ||
rs6983267 | 0.578 | 0.440 | 8 | 127401060 | non coding transcript exon variant | G/T | snv | 0.37 | 13 | ||
rs34612342 | 0.653 | 0.400 | 1 | 45332803 | missense variant | T/C | snv | 1.5E-03 | 1.6E-03 | 11 | |
rs7014346 | 0.732 | 0.240 | 8 | 127412547 | intron variant | A/G | snv | 0.63 | 11 | ||
rs540635787 | 0.851 | 0.200 | 22 | 28694073 | missense variant | G/A;C;T | snv | 1.7E-05 | 4 | ||
rs7837328 | 0.882 | 0.120 | 8 | 127410882 | intron variant | A/G | snv | 0.52 | 2 |