Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs63750231 | 0.689 | 0.160 | 14 | 73198100 | missense variant | A/C;G | snv | 23 | |||
rs781049584 | 0.724 | 0.280 | 21 | 26021917 | missense variant | T/G | snv | 8.2E-06 | 7.0E-06 | 18 | |
rs572842823 | 0.763 | 0.160 | 21 | 25897626 | missense variant | T/A;G | snv | 11 | |||
rs371425292 | 0.763 | 0.160 | 21 | 25897627 | missense variant | C/A;T | snv | 8.0E-06 | 10 | ||
rs63750526 | 0.776 | 0.160 | 14 | 73192832 | missense variant | C/A | snv | 10 | |||
rs63750847 | 0.790 | 0.120 | 21 | 25897620 | missense variant | C/T | snv | 4.5E-04 | 3.0E-04 | 8 | |
rs63751039 | 0.776 | 0.200 | 21 | 25891855 | missense variant | T/C | snv | 8 |