| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs61732239 | 1.000 | 0.120 | 20 | 44625622 | missense variant | C/G;T | snv | 1.0E-03 | 2 | ||
| rs128621195 | 1.000 | 0.120 | X | 101358672 | missense variant | T/C | snv | 2 | |||
| rs746540053 | 1.000 | 0.040 | 1 | 207911034 | missense variant | C/T | snv | 2 | |||
| rs201137953 | 2 | 162039019 | missense variant | T/A;C | snv | 4.0E-06 | 1 | ||||
| rs2204985 | 14 | 22448641 | intron variant | G/A | snv | 0.52 | 1 | ||||
| rs1336343565 | 11 | 36592848 | missense variant | G/T | snv | 7.0E-06 | 1 |