| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs121908065 | 0.851 | 0.080 | 17 | 4933119 | missense variant | C/T | snv | 2 | |||
| rs1394634674 | 0.925 | 0.080 | 17 | 4933277 | missense variant | T/A | snv | 4.0E-06 | 1 | ||
| rs121908063 | 0.882 | 0.080 | 17 | 4932821 | missense variant | C/T | snv | 1 | |||
| rs771048666 | 1.000 | 0.080 | 17 | 4933038 | missense variant | T/C | snv | 1.2E-04 | 1.3E-04 | 1 | |
| rs781541857 | 1.000 | 0.080 | 17 | 4932845 | missense variant | T/C | snv | 1 | |||
| rs121909751 | 1.000 | 0.080 | 22 | 19724240 | missense variant | G/C | snv | 1 | |||
| rs121918036 | 0.925 | 0.080 | 3 | 129061849 | missense variant | A/G | snv | 1 | |||
| rs121918037 | 0.882 | 0.080 | 3 | 129061951 | missense variant | T/C;G | snv | 4.0E-06 | 1 | ||
| rs121918038 | 0.925 | 0.080 | 3 | 129061759 | missense variant | T/C | snv | 1 | |||
| rs28933377 | 0.925 | 0.080 | 3 | 129061906 | missense variant | T/C | snv | 6.9E-05 | 8.4E-05 | 1 | |
| rs28933378 | 0.925 | 0.080 | 3 | 129061809 | missense variant | T/C | snv | 7.8E-05 | 7.0E-06 | 1 | |
| rs5030764 | 0.882 | 0.080 | 3 | 129061921 | missense variant | A/G | snv | 4.8E-04 | 7.4E-04 | 1 | |
| rs121909750 | 1.000 | 0.080 | 22 | 19724181 | missense variant | A/G;T | snv | 4.2E-04 | 1 |