| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs61753038 | 0.851 | 0.080 | 1 | 94005470 | stop gained | G/A | snv | 1.2E-05 | 7.0E-06 | 1 | |
| rs61751402 | 0.882 | 0.080 | 1 | 94029515 | missense variant | C/T | snv | 6.3E-05 | 5.6E-05 | 1 | |
| rs1801269 | 0.851 | 0.080 | 1 | 94041345 | missense variant | C/A;T | snv | 3.1E-04; 4.0E-06 | 1 | ||
| rs61753033 | 0.882 | 0.080 | 1 | 94008767 | missense variant | A/G | snv | 2.0E-05 | 1 | ||
| rs61751392 | 0.827 | 0.080 | 1 | 94063250 | missense variant | A/G | snv | 1.5E-04 | 1.7E-04 | 1 | |
| rs779426136 | 0.925 | 0.120 | 1 | 94041346 | missense variant | G/A;T | snv | 1.2E-05; 4.0E-06 | 1 | ||
| rs481931 | 0.882 | 0.120 | 1 | 94104460 | intron variant | G/T | snv | 0.32 | 1 | ||
| rs61750654 | 0.925 | 0.120 | 1 | 94000870 | stop gained | G/A | snv | 2.0E-05 | 7.0E-06 | 1 | |
| rs61751374 | 0.776 | 0.160 | 1 | 94043413 | missense variant | G/A | snv | 1.7E-03 | 1.7E-03 | 5 | |
| rs61750120 | 0.882 | 0.160 | 1 | 94042767 | missense variant | G/A | snv | 1.2E-04 | 1.8E-04 | 3 | |
| rs61748537 | 0.882 | 0.160 | 1 | 94098906 | missense variant | C/G;T | snv | 4.0E-05; 8.0E-06 | 2 | ||
| rs560426 | 0.851 | 0.200 | 1 | 94087882 | intron variant | C/T | snv | 0.53 | 5 | ||
| rs1800553 | 0.742 | 0.240 | 1 | 94008251 | missense variant | C/T | snv | 4.7E-03 | 3.0E-03 | 13 |