| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs778040733 | 1.000 | 0.080 | 4 | 109988662 | missense variant | T/C | snv | 1.2E-05 | 1.4E-05 | 1 | |
| rs887183646 | 1.000 | 0.080 | 4 | 109976079 | missense variant | C/T | snv | 3.2E-05 | 2.8E-05 | 1 | |
| rs902596253 | 1.000 | 0.080 | 4 | 109941062 | missense variant | C/T | snv | 1 | |||
| rs11568953 | 1.000 | 0.040 | 4 | 109963240 | synonymous variant | A/G | snv | 9.7E-03 | 1.0E-02 | 1 | |
| rs4444903 | 0.630 | 0.360 | 4 | 109912954 | 5 prime UTR variant | A/G | snv | 0.51 | 35 | ||
| rs769047429 | 1.000 | 4 | 109999827 | frameshift variant | -/G | delins | 8.0E-06 | 1 | |||
| rs3756261 | 0.925 | 0.160 | 4 | 109911150 | upstream gene variant | T/C | snv | 9.9E-02 | 2 | ||
| rs11568835 | 1.000 | 0.120 | 4 | 109911514 | upstream gene variant | G/A | snv | 2.7E-02 | 1 |