Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs147105770 | 0.776 | 0.280 | 16 | 13935697 | missense variant | C/G;T | snv | 1.2E-05; 6.4E-05 | 5 | ||
rs121913049 | 0.851 | 0.240 | 16 | 13947991 | missense variant | C/G;T | snv | 4.8E-04 | 2 | ||
rs121913050 | 0.882 | 0.240 | 16 | 13926630 | missense variant | G/A;C;T | snv | 2.4E-05; 4.0E-06; 4.0E-06 | 1 |