Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1569167607 | 1.000 | 0.040 | 22 | 37973727 | stop gained | G/C | snv | 3 | |||
rs74315515 | 0.925 | 0.240 | 22 | 37983381 | missense variant | C/G;T | snv | 2 | |||
rs1569169289 | 1.000 | 0.040 | 22 | 37978077 | stop gained | G/A | snv | 1 | |||
rs750566714 | 1.000 | 0.040 | 22 | 37978082 | missense variant | C/T | snv | 7.0E-06 | 1 | ||
rs1057518656 | 1.000 | 0.040 | 22 | 37983469 | missense variant | G/C | snv | 1 |