Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2476601 | 0.498 | 0.800 | 1 | 113834946 | missense variant | A/G | snv | 0.93 | 0.93 | 13 | |
rs2187668 | 0.701 | 0.480 | 6 | 32638107 | intron variant | C/T | snv | 3.3E-03 | 10 | ||
rs9268853 | 0.790 | 0.440 | 6 | 32461866 | intron variant | T/C | snv | 0.29 | 8 | ||
rs2305480 | 0.763 | 0.280 | 17 | 39905943 | missense variant | G/A | snv | 0.40 | 0.35 | 7 | |
rs2872507 | 0.752 | 0.360 | 17 | 39884510 | intergenic variant | G/A;T | snv | 7 | |||
rs2327832 | 0.790 | 0.320 | 6 | 137651931 | intergenic variant | A/G | snv | 0.16 | 6 | ||
rs9272346 | 0.790 | 0.320 | 6 | 32636595 | intron variant | G/A | snv | 0.54 | 6 | ||
rs3129890 | 0.827 | 0.280 | 6 | 32446496 | downstream gene variant | T/A;C | snv | 5 | |||
rs7775228 | 0.790 | 0.360 | 6 | 32690302 | TF binding site variant | T/C | snv | 0.15 | 5 | ||
rs3117098 | 0.851 | 0.280 | 6 | 32390736 | non coding transcript exon variant | G/A | snv | 0.72 | 4 | ||
rs3129943 | 0.851 | 0.240 | 6 | 32370918 | intron variant | A/G | snv | 0.26 | 4 | ||
rs3763309 | 0.882 | 0.160 | 6 | 32408196 | upstream gene variant | C/A;T | snv | 3 | |||
rs9268516 | 0.882 | 0.200 | 6 | 32411712 | upstream gene variant | C/T | snv | 0.24 | 3 | ||
rs987870 | 0.851 | 0.160 | 6 | 33075103 | intron variant | A/G | snv | 0.19 | 3 | ||
rs881375 | 0.925 | 0.160 | 9 | 120890620 | intron variant | T/C | snv | 0.68 | 2 | ||
rs9275698 | 0.925 | 0.160 | 6 | 32720196 | downstream gene variant | A/G | snv | 0.37 | 2 |