Source: ALL
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs76763715 | 0.658 | 0.520 | 1 | 155235843 | missense variant | T/C;G | snv | 2.3E-03 | 35 | ||
| rs421016 | 0.683 | 0.440 | 1 | 155235252 | missense variant | A/C;G | snv | 8.0E-06; 1.3E-03 | 30 | ||
| rs1289324472 | 0.716 | 0.400 | 1 | 155236354 | missense variant | T/C | snv | 1.4E-05 | 21 | ||
| rs2230288 | 0.776 | 0.160 | 1 | 155236376 | missense variant | C/T | snv | 1.0E-02 | 1.0E-02 | 18 | |
| rs75822236 | 0.752 | 0.200 | 1 | 155235002 | missense variant | C/T | snv | 1.8E-04 | 6.1E-05 | 10 | |
| rs387906315 | 0.790 | 0.160 | 1 | 155240660 | frameshift variant | -/C | delins | 5.2E-05 | 5.6E-05 | 8 | |
| rs75548401 | 0.882 | 0.160 | 1 | 155236246 | missense variant | G/A | snv | 5.9E-03 | 6.2E-03 | 6 | |
| rs1317187144 | 0.851 | 0.120 | 1 | 155239889 | missense variant | T/C | snv | 4.0E-06 | 4 | ||
| rs439898 | 0.882 | 0.120 | 1 | 155238630 | missense variant | G/A | snv | 2.8E-05 | 3 | ||
| rs80356773 | 0.925 | 0.080 | 1 | 155235002 | missense variant | C/T | snv | 3 | |||
| rs1296507371 | 0.925 | 0.120 | 1 | 155237433 | missense variant | G/T | snv | 4.0E-06 | 2 | ||
| rs1064648 | 1.000 | 0.040 | 1 | 155236366 | missense variant | C/T | snv | 6.0E-05 | 2.1E-05 | 1 | |
| rs1191051168 | 1.000 | 0.040 | 1 | 155237408 | missense variant | G/C | snv | 4.0E-06 | 7.0E-06 | 1 | |
| rs374117599 | 1.000 | 0.040 | 1 | 155237439 | missense variant | G/A | snv | 3.6E-05 | 2.1E-05 | 1 | |
| rs374306700 | 1.000 | 0.040 | 1 | 155236367 | missense variant | G/A | snv | 1.2E-05 | 1 |