Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs4835265 | 4 | 145900258 | intron variant | C/A | snv | 0.15 | 1 | ||||
rs11066453 | 1.000 | 0.080 | 12 | 112927816 | intron variant | A/G | snv | 3.8E-03 | 2 | ||
rs2393791 | 0.925 | 0.160 | 12 | 120986153 | intron variant | C/T | snv | 0.62 | 3 | ||
rs4820599 | 0.925 | 0.160 | 22 | 24594246 | intron variant | A/G | snv | 0.43 | 3 | ||
rs12539316 | 0.925 | 0.120 | 7 | 73563568 | downstream gene variant | A/G | snv | 0.28 | 5 | ||
rs12229654 | 0.763 | 0.320 | 12 | 110976657 | intergenic variant | T/G | snv | 4.8E-03 | 10 | ||
rs2074356 | 0.763 | 0.280 | 12 | 112207597 | intron variant | G/A | snv | 3.8E-03 | 12 |