Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs6570507 | 0.827 | 0.240 | 6 | 142358435 | intron variant | G/A | snv | 0.47 | 11 | ||
rs11205303 | 0.882 | 0.120 | 1 | 149934520 | missense variant | T/C | snv | 0.33 | 0.29 | 9 | |
rs7741741 | 0.925 | 0.040 | 6 | 142334664 | intron variant | T/A;G | snv | 6 | |||
rs10739217 | 0.925 | 0.040 | 9 | 105973112 | regulatory region variant | T/A;C | snv | 3 |