| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs371854396 | 1.000 | 0.040 | 1 | 20638098 | missense variant | C/G;T | snv | 1.6E-05; 4.0E-06 | 1 | ||
| rs74315360 | 0.925 | 0.040 | 1 | 20638104 | missense variant | C/A | snv | 1 | |||
| rs768091663 | 1.000 | 0.040 | 1 | 20637956 | missense variant | G/C | snv | 2.0E-05 | 1 | ||
| rs138302371 | 1.000 | 0.040 | 1 | 20638041 | missense variant | C/T | snv | 1.9E-04 | 1.7E-04 | 1 | |
| rs573931674 | 1.000 | 0.040 | 1 | 20639934 | missense variant | G/A | snv | 4.0E-06 | 1 | ||
| rs138050841 | 0.925 | 0.040 | 1 | 20637894 | missense variant | G/A | snv | 2.0E-05 | 3.5E-05 | 1 | |
| rs28940284 | 1.000 | 0.040 | 1 | 20644526 | missense variant | C/A;T | snv | 4.0E-06 | 1 | ||
| rs764328076 | 1.000 | 0.040 | 1 | 20649134 | missense variant | G/A | snv | 2.4E-05 | 7.0E-06 | 1 | |
| rs772510148 | 1.000 | 0.040 | 1 | 20644551 | missense variant | G/A | snv | 4.4E-05 | 2.1E-05 | 1 | |
| rs74315358 | 1.000 | 0.040 | 1 | 20644549 | missense variant | G/A | snv | 4.4E-05 | 7.7E-05 | 1 | |
| rs74315359 | 0.882 | 0.040 | 1 | 20644651 | missense variant | C/T | snv | 2.0E-05 | 1.4E-05 | 1 | |
| rs28940285 | 1.000 | 0.040 | 1 | 20645640 | missense variant | T/C | snv | 1.6E-05 | 3.5E-05 | 1 | |
| rs1195888869 | 1.000 | 0.040 | 1 | 20645706 | missense variant | T/C | snv | 4.0E-06 | 1 | ||
| rs775809722 | 1.000 | 0.040 | 1 | 20633925 | missense variant | A/C;G | snv | 5.3E-06; 3.7E-05 | 1 | ||
| rs556540177 | 1.000 | 0.040 | 1 | 20648601 | missense variant | G/A;C;T | snv | 1.0E-04; 4.0E-06; 1.6E-05 | 1 | ||
| rs74315355 | 0.790 | 0.080 | 1 | 20644639 | missense variant | G/A | snv | 1 | |||
| rs372280083 | 1.000 | 0.040 | 1 | 20644515 | missense variant | C/G | snv | 9.5E-05 | 5.6E-05 | 1 |