| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1057516085 | 0.827 | 0.080 | 20 | 63444747 | missense variant | C/T | snv | 8 | |||
| rs886041715 | 0.827 | 0.040 | 16 | 56192353 | missense variant | G/A;C;T | snv | 7 | |||
| rs796052650 | 0.925 | 0.040 | 20 | 63413574 | missense variant | G/A;C | snv | 4 | |||
| rs1057518443 | 1.000 | 0.040 | X | 120557964 | missense variant | T/C | snv | 3 | |||
| rs1057524792 | 1.000 | 0.040 | 4 | 39467617 | missense variant | T/G | snv | 3 | |||
| rs751866383 | 1.000 | 0.040 | 4 | 39470047 | missense variant | G/T | snv | 4.0E-06 | 3 | ||
| rs866291718 | 1.000 | 0.040 | 4 | 39470042 | missense variant | A/G | snv | 3 | |||
| rs961150638 | 1.000 | 0.040 | 4 | 39470038 | missense variant | G/C | snv | 4.0E-06 | 3 | ||
| rs771844443 | 1.000 | 0.040 | 2 | 165309194 | missense variant | A/G | snv | 4.0E-06 | 3 | ||
| rs796053150 | 1.000 | 0.040 | 2 | 165386827 | missense variant | A/G | snv | 3 |