| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs137854539 | 0.716 | 0.520 | 20 | 58903703 | missense variant | C/T | snv | 28 | |||
| rs7121 | 0.882 | 0.160 | 20 | 58903752 | missense variant | C/G;T | snv | 0.54 | 6 | ||
| rs757110000 | 1.000 | 0.080 | 20 | 58905388 | synonymous variant | C/T | snv | 1.2E-05 | 7.0E-06 | 1 | |
| rs104894585 | 0.851 | 0.120 | 17 | 70175263 | missense variant | C/G;T | snv | 5 | |||
| rs587782927 | 0.882 | 0.080 | 6 | 7574084 | splice region variant | AG/- | delins | 4 | |||
| rs200745877 | 1.000 | 0.080 | 6 | 7580307 | missense variant | A/G | snv | 6.8E-05 | 6.3E-05 | 1 |