Source: CURATED
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1801177 | 0.742 | 0.240 | 8 | 19948197 | missense variant | G/A;C | snv | 1.4E-02; 2.0E-05 | 1 | ||
| rs268 | 0.637 | 0.480 | 8 | 19956018 | missense variant | A/G | snv | 1.3E-02 | 1.3E-02 | 6 | |
| rs118204057 | 0.732 | 0.400 | 8 | 19954222 | missense variant | G/A;C | snv | 1.9E-04 | 2 | ||
| rs145657341 | 0.925 | 0.120 | 8 | 19951811 | missense variant | G/A | snv | 1.7E-04 | 7.0E-05 | 1 | |
| rs118204082 | 0.851 | 0.120 | 8 | 19955863 | missense variant | C/G;T | snv | 1.5E-04 | 1 | ||
| rs371282890 | 0.827 | 0.120 | 8 | 19955900 | missense variant | C/G | snv | 1.1E-04 | 6.3E-05 | 1 | |
| rs373088068 | 1.000 | 0.080 | 8 | 19951805 | missense variant | G/C | snv | 9.9E-05 | 1.3E-04 | 1 | |
| rs149089920 | 0.925 | 0.120 | 8 | 19962134 | missense variant | G/A | snv | 6.0E-05 | 2.1E-04 | 1 | |
| rs1800011 | 1.000 | 0.080 | 8 | 19955927 | missense variant | G/A;C | snv | 6.0E-05 | 1 | ||
| rs118204060 | 0.807 | 0.160 | 8 | 19954279 | missense variant | C/T | snv | 4.0E-05 | 1.4E-05 | 1 | |
| rs528243561 | 1.000 | 0.080 | 8 | 19954258 | missense variant | T/A;C | snv | 3.6E-05 | 1 | ||
| rs546542623 | 1.000 | 0.080 | 8 | 19959335 | missense variant | C/T | snv | 2.0E-05 | 1 | ||
| rs118204080 | 1.000 | 0.080 | 8 | 19954333 | missense variant | T/C | snv | 2.0E-05 | 1 | ||
| rs118204068 | 0.925 | 0.120 | 8 | 19955894 | missense variant | G/A | snv | 1.6E-05 | 1.4E-05 | 1 | |
| rs118204061 | 1.000 | 0.080 | 8 | 19954240 | missense variant | T/C | snv | 1.6E-05 | 4.2E-05 | 1 | |
| rs35414700 | 1.000 | 0.080 | 8 | 19955901 | missense variant | T/G | snv | 1.2E-05 | 1.4E-05 | 1 | |
| rs761265900 | 1.000 | 0.080 | 8 | 19956040 | missense variant | C/G | snv | 1.2E-05 | 7.0E-06 | 1 | |
| rs118204076 | 1.000 | 0.080 | 8 | 19954199 | missense variant | C/G;T | snv | 1.2E-05 | 1 | ||
| rs757546424 | 1.000 | 0.080 | 8 | 19954236 | missense variant | A/C | snv | 1.2E-05 | 1 | ||
| rs766134215 | 1.000 | 0.080 | 8 | 19939529 | splice donor variant | G/C;T | snv | 8.7E-06; 4.4E-06; 4.4E-06 | 1 | ||
| rs118204077 | 1.000 | 0.080 | 8 | 19955873 | missense variant | C/T | snv | 8.0E-06 | 7.0E-06 | 1 | |
| rs1409123950 | 1.000 | 0.080 | 8 | 19955994 | missense variant | G/A | snv | 8.0E-06 | 1 | ||
| rs118204058 | 1.000 | 0.080 | 8 | 19951916 | stop gained | C/G;T | snv | 4.0E-06; 8.0E-06 | 1 | ||
| rs770601263 | 1.000 | 0.080 | 8 | 19954273 | missense variant | T/G | snv | 8.0E-06 | 1 | ||
| rs118204062 | 1.000 | 0.080 | 8 | 19955874 | missense variant | G/A | snv | 4.0E-06 | 1.4E-05 | 1 |