Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs869320686 | 0.882 | 22 | 20990476 | missense variant | G/A | snv | 5 | ||||
rs148677674 | 0.882 | 0.160 | 22 | 20994988 | missense variant | C/A;T | snv | 2.4E-05; 1.6E-04 | 3 | ||
rs189150283 | 0.925 | 22 | 20992304 | stop gained | C/T | snv | 6.0E-05 | 7.0E-05 | 3 | ||
rs797045165 | 0.925 | 22 | 20991686 | missense variant | C/T | snv | 7.0E-06 | 2 | |||
rs1223430276 | 1.000 | 22 | 20991684 | missense variant | G/A | snv | 7.0E-06 | 1 | |||
rs797045166 | 1.000 | 22 | 20990474 | missense variant | G/A | snv | 1 |