| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs7449334 | 1.000 | 0.040 | 5 | 91046595 | intron variant | G/A;C | snv | 0.76 | 2 | ||
| rs62374016 | 5 | 90915456 | intron variant | T/C | snv | 0.25 | 1 | ||||
| rs57190680 | 5 | 90910368 | intron variant | C/A | snv | 0.23 | 1 | ||||
| rs6860111 | 5 | 90967764 | intron variant | T/G | snv | 0.50 | 1 | ||||
| rs2247870 | 1.000 | 0.040 | 5 | 90855772 | missense variant | G/A | snv | 0.54 | 0.45 | 1 | |
| rs2247419 | 1.000 | 0.040 | 5 | 90859597 | intron variant | A/G | snv | 0.57 | 1 | ||
| rs74501188 | 1.000 | 0.080 | 5 | 90931162 | 5 prime UTR variant | G/A | snv | 0.17 | 1 | ||
| rs3105793 | 5 | 90930244 | intron variant | G/A | snv | 0.25 | 1 | ||||
| rs11744148 | 5 | 90933990 | intron variant | G/A | snv | 0.18 | 1 | ||||
| rs4916831 | 1.000 | 0.040 | 5 | 90916459 | intron variant | A/G | snv | 0.44 | 1 | ||
| rs4489092 | 5 | 91124827 | intron variant | G/T | snv | 0.49 | 1 | ||||
| rs13357230 | 5 | 91115255 | intron variant | A/G | snv | 5.8E-02 | 1 | ||||
| rs59661306 | 1.000 | 0.080 | 5 | 91087644 | intron variant | A/G | snv | 0.18 | 1 |