| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs730880179 | 0.925 | 0.120 | 12 | 32896556 | missense variant | T/A | snv | 6.0E-05 | 1.5E-04 | 2 | |
| rs7121 | 0.882 | 0.160 | 20 | 58903752 | missense variant | C/G;T | snv | 0.54 | 6 | ||
| rs12143842 | 0.925 | 0.160 | 1 | 162064100 | intergenic variant | C/T | snv | 0.22 | 3 | ||
| rs3766871 | 0.790 | 0.240 | 1 | 237614784 | missense variant | G/A;T | snv | 4.0E-02 | 9 | ||
| rs374528680 | 0.851 | 0.240 | 12 | 2686216 | missense variant | G/A;C | snv | 4.0E-06; 6.0E-05 | 5 | ||
| rs137854539 | 0.716 | 0.520 | 20 | 58903703 | missense variant | C/T | snv | 28 |