Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1701704 | 0.851 | 0.200 | 12 | 56018703 | intron variant | T/G | snv | 0.25 | 5 | ||
rs1893217 | 0.742 | 0.440 | 18 | 12809341 | intron variant | A/G | snv | 0.12 | 8 | ||
rs2187668 | 0.701 | 0.480 | 6 | 32638107 | intron variant | C/T | snv | 3.3E-03 | 10 | ||
rs2290400 | 0.790 | 0.360 | 17 | 39909987 | intron variant | T/C | snv | 0.48 | 6 | ||
rs241425 | 0.925 | 0.160 | 6 | 32837132 | intron variant | A/C;G | snv | 2 | |||
rs2542151 | 0.763 | 0.480 | 18 | 12779948 | upstream gene variant | G/T | snv | 0.83 | 6 | ||
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 | ||
rs3134792 | 0.851 | 0.280 | 6 | 31344549 | intron variant | T/G | snv | 8.8E-02 | 3 | ||
rs404860 | 0.925 | 0.160 | 6 | 32216568 | non coding transcript exon variant | T/C | snv | 0.21 | 2 | ||
rs4505848 | 0.776 | 0.400 | 4 | 122211337 | intron variant | A/G | snv | 0.29 | 2 | ||
rs7775228 | 0.790 | 0.360 | 6 | 32690302 | TF binding site variant | T/C | snv | 0.15 | 5 | ||
rs9272346 | 0.790 | 0.320 | 6 | 32636595 | intron variant | G/A | snv | 0.54 | 6 | ||
rs2476601 | 0.498 | 0.800 | 1 | 113834946 | missense variant | A/G | snv | 0.93 | 0.93 | 13 |